MCID: HRD018
MIFTS: 42

Hair Disease

Categories: Rare diseases, Skin diseases
Data Licensing
For inquiries, contact:

Aliases & Classifications for Hair Disease

MalaCards integrated aliases for Hair Disease:

Name: Hair Disease 11 14 75
Hair Diseases 43 71
Hair Disorder 53
Hair Problems 41
Hair Anomaly 58

Classifications:

Orphanet: 58  
Rare skin diseases


External Ids:

Disease Ontology 11 DOID:421
MeSH 43 D006201
NCIt 49 C34656
SNOMED-CT 68 267862002
UMLS via Orphanet 72 C0265991
Orphanet 58 ORPHA79363
UMLS 71 C0018500

Summaries for Hair Disease

MedlinePlus: 41 The average person has 5 million hairs. Hair grows all over your body except on your lips, palms, and the soles of your feet. It takes about a month for healthy hair to grow half an inch. Most hairs grow for up to six years and then fall out. New hairs grow in their place. Hair helps keep you warm. It also protects your eyes, ears and nose from small particles in the air. Common problem with the hair and scalp include hair loss, infections, and flaking.

MalaCards based summary: Hair Disease, also known as hair diseases, is related to hypotrichosis 7 and monilethrix, and has symptoms including pruritus and exanthema. An important gene associated with Hair Disease is KRT86 (Keratin 86), and among its related pathways/superpathways are Keratinization and Innate Lymphoid Cells Differentiation. The drugs Eflornithine and Ornithine have been mentioned in the context of this disorder. Affiliated tissues include hair, skin and cortex, and related phenotype is integument.

Disease Ontology: 11 An integumentary system disease that is located in hair.

Wikipedia: 75 Hair diseases are disorders primarily associated with the follicles of the hair. A few examples... more...

Related Diseases for Hair Disease

Diseases in the Hair Disease family:

Hair-an Syndrome

Diseases related to Hair Disease via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 442, show less)
# Related Disease Score Top Affiliating Genes
1 hypotrichosis 7 32.0 LPAR6 LIPH KRT74 DSG4
2 monilethrix 32.0 LPAR6 LIPH KRT86 KRT83 KRT81 KRT74
3 familial woolly hair syndrome 31.8 LPAR6 LIPH KRT86 KRT83 KRT81 KRT74
4 hypotrichosis 31.7 LPAR6 LIPH KRT86 KRT83 KRT74 DSG4
5 seborrheic dermatitis 30.5 SHBG CD4 CCR6
6 androgenic alopecia 30.4 SRD5A2 SHBG KRT15
7 ectodermal dysplasia 30.3 KRT74 H2AC18 DSP AIRE
8 alopecia, androgenetic, 1 30.3 SRD5A2 SHBG
9 ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive 30.2 KRT86 KRT83 KRT74
10 alopecia 30.2 SRD5A2 SHBG KRT86 KRT83 KRT15 DSP
11 telangiectasis 30.2 H2AC18 ERCC6 CCR6
12 contact dermatitis 30.2 CD8A CD4 CCR6
13 telogen effluvium 30.0 SRD5A2 SHBG
14 skin disease 30.0 H2AC18 ERCC6 DSP DSG4 CSF3 CD8A
15 menkes disease 11.5
16 ringed hair 11.2
17 hairy elbows 11.1
18 genetic hair anomaly 11.1
19 loose anagen hair syndrome 11.0
20 nevus, epidermal 10.9
21 noonan syndrome-like disorder with loose anagen hair 1 10.9
22 familial isolated trichomegaly 10.9
23 clouston syndrome 10.9
24 pseudofolliculitis barbae 10.8
25 hypertrichosis 10.8
26 acquired kinky hair syndrome 10.8
27 cutaneous candidiasis 10.5 CCR6 AIRE
28 hilar lung neoplasm 10.5 CD8A CD4
29 hypotrichosis simplex 10.5 LPAR6 LIPH DSG4
30 hypotrichosis, congenital, with juvenile macular dystrophy 10.5 LPAR6 LIPH DSG4
31 gastroduodenitis 10.5 CD8A CD4 CCR6
32 spongiotic dermatitis 10.5 CD8A CD4 CCR6
33 skin sarcoidosis 10.5 CD8A CD4 CCR6
34 autoimmune cholangitis 10.5 CD8A CD4 CCR6
35 farmer's lung 10.5 CD8A CD4 CCR6
36 multicentric castleman disease 10.5 H2AC18 CD4 CCR6
37 focal chorioretinitis 10.5 CD4 AIRE
38 evans' syndrome 10.5 CD8A CD4 CCR6
39 progressive relapsing multiple sclerosis 10.5 CD8A CD4 CCR6
40 oral tuberculosis 10.5 CD8A CD4
41 wissler-fanconi syndrome 10.5 CD8A CD4 AIRE
42 dacryoadenitis 10.5 CD8A CD4 CCR6
43 scabies 10.5 CD8A CD4 CCR6
44 naegeli-franceschetti-jadassohn syndrome 10.5 KRT86 KRT83 KRT74
45 iritis 10.5 CD8A CD4 CCR6
46 non-severe covid-19 10.5 CD8A CD4 CCR6
47 early yaws 10.5 CD8A CD4
48 diffuse alopecia areata 10.5 LIPH KRT86
49 woolly hair, autosomal dominant 10.5 LPAR6 LIPH KRT74
50 hypotrichosis 3 10.5 LPAR6 LIPH KRT74
51 mite infestation 10.5 CD8A CD4 CCR6
52 autoimmune glomerulonephritis 10.5 CD8A CD4 CCR6
53 fungal meningitis 10.5 CD8A CD4 CCR6
54 tuberculoid leprosy 10.5 CD8A CD4 CCR6
55 xerophthalmia 10.5 CD8A CD4 CCR6
56 immunodeficiency 14 10.5 CD8A CD4 CCR6
57 immunodeficiency 16 10.5 CD8A CD4 CCR6
58 nonspecific interstitial pneumonia 10.5 CD8A CD4 CCR6
59 hypotrichosis 4 10.5 LPAR6 LIPH KRT74
60 hantavirus hemorrhagic fever with renal syndrome 10.5 CD8A CD4 CCR6
61 long covid 10.5 CD8A CD4 CCR6
62 thymic dysplasia 10.5 CD8A CD4 AIRE
63 cryptococcal meningitis 10.5 CD8A CD4 CCR6
64 anal squamous cell carcinoma 10.5 H2AC18 CD8A CD4
65 xeroderma pigmentosum, complementation group f 10.5 H2AC18 ERCC6 ERCC3
66 follicular mucinosis 10.5 KRT15 CD8A CD4
67 xeroderma pigmentosum, complementation group c 10.5 H2AC18 ERCC6 ERCC3
68 chorioretinitis 10.5 CD8A CD4 CCR6
69 autoimmune peripheral neuropathy 10.5 CD8A CD4 AIRE
70 transverse myelitis 10.5 CD8A CD4 CCR6
71 aortitis 10.5 CSF3 CD4 CCR6
72 genital herpes 10.5 CD8A CD4 CCR6
73 cecal disease 10.5 H2AC18 CD4 CCR6
74 acute disseminated encephalomyelitis 10.5 CD8A CD4 CCR6
75 birdshot chorioretinopathy 10.5 CD8A CD4 CCR6
76 mucocutaneous leishmaniasis 10.5 H2AC18 CD8A CD4
77 tularemia 10.5 CD8A CD4 CCR6
78 crescentic glomerulonephritis 10.5 CD8A CD4 CCR6
79 primary systemic mycosis 10.5 CD8A CD4 CCR6
80 immune-complex glomerulonephritis 10.5 H2AC18 CD8A CD4
81 ventilation pneumonitis 10.5 CD8A CD4
82 central nervous system vasculitis 10.5 CD8A CD4 CCR6
83 parasitic ectoparasitic infectious disease 10.5 CD8A CD4 CCR6
84 acute proliferative glomerulonephritis 10.5 CD8A CD4 CCR6
85 human cytomegalovirus infection 10.5 CD8A CD4 CCR6
86 extrapulmonary tuberculosis 10.5 CD8A CD4 CCR6
87 t-cell immunodeficiency, congenital alopecia, and nail dystrophy 10.5 LPAR6 LIPH KRT86 DSG4
88 intestinal perforation 10.5 CD8A CD4 CCR6
89 autoimmune disease of eyes, ear, nose and throat 10.5 CD8A CD4 CCR6
90 goodpasture syndrome 10.5 H2AC18 CD4 CCR6
91 xeroderma pigmentosum, complementation group a 10.5 H2AC18 ERCC6 ERCC3
92 rothmund-thomson syndrome, type 2 10.5 H2AC18 ERCC6 ERCC3
93 autoimmune polyendocrine syndrome type 1 10.5 CD4 CCR6 AIRE
94 autoimmune polyendocrine syndrome 10.5 CD4 CCR6 AIRE
95 primary thrombocytopenia 10.5 CD8A CD4 CCR6
96 t-cell adult acute lymphocytic leukemia 10.5 CD8A CD4 CCR6
97 adult acute lymphocytic leukemia 10.5 CD8A CD4 CCR6
98 alopecia universalis congenita 10.5 CD8A CD4 AIRE
99 blepharitis 10.5 CD8A CD4 CCR6
100 autoimmune uveitis 10.5 CD8A CD4 CCR6
101 dengue hemorrhagic fever 10.5 CD8A CD4 CCR6
102 vaginal disease 10.5 CD8A CD4 CCR6
103 t cell deficiency 10.5 CD8A CD4 CCR6
104 bullous skin disease 10.5 DSP DSG4 CD4 CCR6
105 pernicious anemia 10.5 CD4 CCR6 AIRE
106 t-cell immunodeficiency with thymic aplasia 10.5 CD8A CD4 AIRE
107 giardiasis 10.5 H2AC18 CD8A CD4
108 progressive multifocal leukoencephalopathy 10.5 CD8A CD4 CCR6
109 anterior uveitis 10.5 CD8A CD4 CCR6
110 pemphigus vulgaris, familial 10.5 DSP DSG4 CCR6
111 lepromatous leprosy 10.5 CD8A CD4 CCR6
112 herpangina 10.5 CD8A CD4 CCR6
113 angioimmunoblastic t-cell lymphoma 10.5 CD8A CD4 CCR6
114 immunoglobulin alpha deficiency 10.5 CD8A CD4 CCR6
115 diffuse infiltrative lymphocytosis syndrome 10.5 CD8A CD4
116 localized scleroderma 10.5 H2AC18 CD8A CD4
117 lichen disease 10.5 CD8A CD4 CCR6
118 viral meningitis 10.5 CD8A CD4 CCR6
119 viral encephalitis 10.5 CD8A CD4 CCR6
120 autoimmune lymphoproliferative syndrome, type iia 10.5 CD8A CD4
121 cryptococcosis 10.5 CD8A CD4 CCR6
122 autoimmune disease of peripheral nervous system 10.5 CD8A CD4 CCR6
123 pericardium disease 10.5 CD8A CD4 CCR6
124 hemorrhagic cystitis 10.5 CSF3 CD8A CD4
125 invasive aspergillosis 10.5 CSF3 CD4 CCR6
126 immunodeficiency with hyper-igm, type 1 10.5 H2AC18 CD4 CCR6
127 gingival disease 10.5 CD8A CD4 CCR6
128 lacrimal apparatus disease 10.5 CD8A CD4 CCR6
129 uv-sensitive syndrome 10.5 H2AC18 ERCC6 ERCC3
130 vogt-koyanagi-harada disease 10.5 CD8A CD4 CCR6
131 avian influenza 10.5 CD8A CD4 CCR6
132 plasma protein metabolism disease 10.5 CD8A CD4 CCR6
133 thrombocytopenia due to platelet alloimmunization 10.5 CD8A CD4 CCR6
134 encephalitozoonosis 10.5 CD8A CD4
135 paranasal sinus disease 10.5 CD8A CD4 CCR6
136 sexual health disorder 10.5 SRD5A2 SHBG H2AC18
137 epidermolytic hyperkeratosis 10.5 KRT86 KRT81 KRT15 DSP
138 felty syndrome 10.5 H2AC18 CSF3 CD8A
139 type 1 diabetes mellitus 23 10.5 CD8A CD4
140 dysentery 10.5 H2AC18 CD4 CCR6
141 panuveitis 10.5 CD8A CD4 CCR6
142 interstitial nephritis 10.5 CD8A CD4 CCR6
143 hypotrichosis 11 10.5 LPAR6 LIPH KRT74 DSG4
144 autoimmune vasculitis 10.5 H2AC18 CD8A CD4 CCR6
145 hypotrichosis 13 10.5 LPAR6 LIPH KRT74 DSG4
146 pachyonychia congenita 1 10.5 KRT86 KRT74 DSP
147 anus cancer 10.5 H2AC18 CD8A CD4 CCR6
148 uterine body mixed cancer 10.5 H2AC18 CD8A CD4
149 autoimmune myocarditis 10.5 H2AC18 CD8A CD4 CCR6
150 autoimmune disease of urogenital tract 10.5 H2AC18 CD8A CD4 CCR6
151 anogenital venereal wart 10.5 H2AC18 CD8A CD4 CCR6
152 orchitis 10.5 H2AC18 CD8A CD4 CCR6
153 conjunctival disease 10.5 CD8A CD4 CCR6
154 t-cell prolymphocytic leukemia 10.5 H2AC18 CD8A CD4
155 fallopian tube disease 10.5 H2AC18 CD8A CD4 CCR6
156 esophageal candidiasis 10.5 CD8A CD4 CCR6 AIRE
157 middle ear disease 10.5 CD8A CD4 CCR6
158 autoimmune gastritis 10.5 CD8A CD4 CCR6 AIRE
159 anus disease 10.5 H2AC18 CD8A CD4 CCR6
160 pharyngitis 10.5 CD8A CD4 CCR6
161 west nile encephalitis 10.5 H2AC18 CD8A CD4 CCR6
162 autoimmune disease of blood 10.5 H2AC18 CD8A CD4 CCR6
163 listeriosis 10.5 H2AC18 CD8A CD4 CCR6
164 autoimmune disease of exocrine system 10.5 H2AC18 CD8A CD4 CCR6
165 splenic disease 10.5 H2AC18 CD8A CD4 CCR6
166 thrombocytopenic purpura, autoimmune 10.5 CD8A CD4 CCR6
167 rectal disease 10.5 H2AC18 CD8A CD4 CCR6
168 ebola hemorrhagic fever 10.5 H2AC18 CD8A CD4 CCR6
169 plague 10.5 H2AC18 CD8A CD4 CCR6
170 spondyloarthropathy 10.5 CD8A CD4 CCR6
171 cockayne syndrome b 10.5 H2AC18 ERCC6 ERCC3
172 coccidiosis 10.5 H2AC18 CD8A CD4 CCR6
173 salivary gland disease 10.5 H2AC18 CD8A CD4 CCR6
174 cork-handlers' disease 10.5 CD8A CD4
175 autoimmune disease of cardiovascular system 10.5 H2AC18 CD8A CD4 CCR6
176 primary progressive multiple sclerosis 10.5 CD8A CD4 CCR6
177 immunodysregulation, polyendocrinopathy, and enteropathy, x-linked 10.5 CD8A CD4 CCR6 AIRE
178 lymph node disease 10.5 H2AC18 CD8A CD4 CCR6
179 oral candidiasis 10.5 CD8A CD4 CCR6 AIRE
180 capillary disease 10.5 CSF3 CD8A CD4
181 commensal bacterial infectious disease 10.5 H2AC18 CD8A CD4 CCR6
182 cranial nerve disease 10.5 ERCC6 CD8A CD4 CCR6
183 woolly hair, autosomal recessive 3 10.5 LPAR6 LIPH
184 blood protein disease 10.5 H2AC18 CD8A CD4 CCR6
185 adult t-cell leukemia/lymphoma 10.5 H2AC18 CD8A CD4 CCR6
186 nail disease 10.5 CD8A CD4 CCR6 AIRE
187 dengue disease 10.5 H2AC18 CD8A CD4 CCR6
188 b cell deficiency 10.5 CD8A CD4 CCR6
189 parasitic helminthiasis infectious disease 10.5 H2AC18 CD8A CD4 CCR6
190 actinic keratosis 10.5 H2AC18 CD8A CD4
191 anemia, autoimmune hemolytic 10.5 CD8A CD4 CCR6
192 endocervical carcinoma 10.5 H2AC18 CD8A CD4
193 xeroderma pigmentosum, complementation group g 10.5 H2AC18 ERCC6 ERCC3
194 mature t-cell and nk-cell lymphoma 10.5 H2AC18 CD8A CD4 CCR6
195 cutaneous leishmaniasis 10.5 H2AC18 CD8A CD4 CCR6
196 extrinsic cardiomyopathy 10.5 H2AC18 CD8A CD4 CCR6
197 chronic asthma 10.5 CD8A CD4 CCR6
198 castleman disease 10.5 KRT15 H2AC18 CD4 CCR6
199 sebaceous gland disease 10.5 SHBG CD4 CCR6
200 chronic fatigue syndrome 10.5 H2AC18 CD8A CD4 CCR6
201 pleural disease 10.5 H2AC18 CD8A CD4 CCR6
202 polyclonal hypergammaglobulinemia 10.5 SLC29A3 CD8A CD4 CCR6
203 syphilis 10.5 CD8A CD4 CCR6
204 aseptic meningitis 10.5 CSF3 CD8A CD4
205 nasal cavity disease 10.5 CD8A CD4 CCR6
206 hepatic vascular disease 10.5 CSF3 CD4 CCR6
207 autoimmune disease of skin and connective tissue 10.5 H2AC18 CD8A CD4 CCR6
208 potocki-shaffer syndrome 10.5 H2AC18 CD8A CD4 CCR6
209 vitiligo-associated multiple autoimmune disease susceptibility 1 10.5 CD8A CD4 CCR6 AIRE
210 adrenal cortex disease 10.5 H2AC18 CD8A CCR6 AIRE
211 hypersensitivity reaction type iv disease 10.5 CD8A CD4 CCR6
212 urinary tract infection 10.5 H2AC18 CD4 CCR6
213 suppurative lymphadenitis 10.5 CD8A CD4
214 critical covid-19 10.5 CSF3 CD8A CD4 CCR6
215 mature b-cell neoplasm 10.5 H2AC18 CD8A CD4 CCR6
216 chronic mucocutaneous candidiasis 10.5 CD8A CD4 CCR6 AIRE
217 sclerosing cholangitis 10.5 CD8A CD4 CCR6
218 parasitic protozoa infectious disease 10.5 H2AC18 CD8A CD4 CCR6
219 hyper ige syndrome 10.5 CD8A CD4 CCR6 AIRE
220 pneumocystosis 10.5 CSF3 CD8A CD4 CCR6
221 viral pneumonia 10.5 CSF3 CD8A CD4 CCR6
222 middle east respiratory syndrome 10.5 CD8A CD4 CCR6
223 mucormycosis 10.5 CSF3 CD8A CD4 CCR6
224 bird fancier's lung 10.5 CD8A CD4
225 respiratory allergy 10.5 CD8A CD4 CCR6
226 visceral leishmaniasis 10.5 H2AC18 CD8A CD4 CCR6
227 bacterial sepsis 10.5 CSF3 CD8A CD4 CCR6
228 spinal cord disease 10.5 H2AC18 CD8A CD4 CCR6
229 aphthous stomatitis 10.5 CSF3 CD8A CD4 CCR6
230 autoimmune disease of gastrointestinal tract 10.5 H2AC18 CD8A CD4 CCR6
231 cockayne syndrome a 10.5 H2AC18 ERCC6 ERCC3
232 chickenpox 10.5 CSF3 CD8A CD4 CCR6
233 cellulitis 10.5 CSF3 CD8A CD4 CCR6
234 keratitis, hereditary 10.5 ERCC6 CD8A CD4 CCR6
235 salmonellosis 10.5 CD8A CD4 CCR6
236 bacterial pneumonia 10.5 CSF3 CD8A CD4 CCR6
237 parapsoriasis 10.5 CD8A CD4
238 meningoencephalitis 10.5 CD8A CD4 CCR6
239 bronchial disease 10.5 H2AC18 CD8A CD4 CCR6
240 panniculitis 10.5 CSF3 CD8A CD4 CCR6
241 primary bacterial infectious disease 10.5 H2AC18 CD8A CD4 CCR6
242 common cold 10.5 CD8A CD4 CCR6
243 severe covid-19 10.5 CSF3 CD8A CD4 CCR6
244 primary syphilis 10.5 CD8A CD4
245 secondary progressive multiple sclerosis 10.5 CD8A CD4 CCR6
246 pfeiffer syndrome 10.5 H2AC18 CD8A CD4 CCR6
247 nose disease 10.5 CD8A CD4 CCR6
248 granulomatous angiitis 10.5 CD8A CD4
249 peripheral t-cell lymphoma 10.5 H2AC18 CD8A CD4 CCR6
250 cryptosporidiosis 10.5 H2AC18 CSF3 CD8A CD4
251 primary cutaneous gamma-delta t-cell lymphoma 10.5 CD8A CD4
252 ovarian cystadenocarcinoma 10.4 H2AC18 ERCC6 CD8A
253 autoimmune disease of central nervous system 10.4 H2AC18 CD8A CD4 CCR6
254 pure red-cell aplasia 10.4 CSF3 CD8A CD4 AIRE
255 herpes zoster 10.4 CD8A CD4 CCR6
256 extrinsic allergic alveolitis 10.4 CD8A CD4 CCR6
257 malignant ovarian surface epithelial-stromal neoplasm 10.4 H2AC18 ERCC6 CD8A CCR6
258 dendritic cell thymoma 10.4 CD4 AIRE
259 colonic benign neoplasm 10.4 H2AC18 CD8A CD4 CCR6
260 crohn's disease 10.4 H2AC18 CD8A CD4 CCR6
261 hemophagocytic lymphohistiocytosis 10.4 CSF3 CD8A CD4 CCR6
262 cervix carcinoma 10.4 H2AC18 CD8A CD4 CCR6
263 systemic scleroderma 10.4 H2AC18 CD8A CD4 CCR6
264 splenic abscess 10.4 CD8A CD4
265 cholangitis, primary sclerosing 10.4 CD8A CD4 CCR6 AIRE
266 mooren's ulcer 10.4 CD8A CD4
267 severe cutaneous adverse reaction 10.4 CD8A CD4 CCR6
268 autoimmune disease of musculoskeletal system 10.4 H2AC18 CD8A CD4 CCR6
269 herpes simplex virus keratitis 10.4 CD8A CD4
270 acute myocarditis 10.4 H2AC18 DSP CD8A CD4 CCR6
271 trypanosomiasis 10.4 H2AC18 CSF3 CD8A CD4
272 bone inflammation disease 10.4 H2AC18 CD8A CD4 CCR6
273 pre-malignant neoplasm 10.4 H2AC18 CD8A CCR6
274 optic nerve disease 10.4 ERCC6 CD8A CD4 CCR6
275 oropharynx cancer 10.4 H2AC18 CD8A CD4
276 allergic disease 10.4 H2AC18 CD8A CD4 CCR6
277 lens disease 10.4 H2AC18 ERCC6 CCR6
278 rectum adenocarcinoma 10.4 CD8A CD4 CCR6
279 adrenal gland disease 10.4 SHBG CCR6 AIRE
280 intestinal benign neoplasm 10.4 H2AC18 ERCC6 CCR6
281 human immunodeficiency virus infectious disease 10.4 H2AC18 CD8A CD4 CCR6
282 uveal disease 10.4 H2AC18 ERCC6 CD8A CD4 CCR6
283 corneal disease 10.4 H2AC18 ERCC6 CD8A CD4 CCR6
284 leprosy 3 10.4 CD8A CD4 CCR6
285 granulomatous dermatitis 10.4 CD8A CD4
286 lymphangioma 10.4 H2AC18 ERCC6 CD8A CD4 CCR6
287 demyelinating disease 10.4 H2AC18 CD8A CD4 CCR6
288 ovary adenocarcinoma 10.4 H2AC18 ERCC6 CD8A
289 mantle cell lymphoma 10.4 H2AC18 CD8A CD4 CCR6
290 uterine corpus cancer 10.4 H2AC18 CD8A CD4
291 hypotrichosis 8 10.4 LPAR6 LIPH KRT83 KRT74 DSG4
292 acute retinal necrosis syndrome 10.4 CD8A CD4
293 autoimmune lymphoproliferative syndrome 10.4 CD8A CD4 CCR6 AIRE
294 thymoma 10.4 DSP CSF3 CD8A AIRE
295 human papillomavirus infectious disease 10.4 CD8A CD4 CCR6
296 disease of mental health 10.4 H2AC18 ERCC6 CD4 CCR6
297 thymus gland disease 10.4 H2AC18 CD8A CD4 CCR6 AIRE
298 thymus cancer 10.4 H2AC18 CD8A CD4 CCR6 AIRE
299 granulomatous hepatitis 10.4 CD8A CD4
300 autoimmune disease of endocrine system 10.4 H2AC18 CD8A CD4 CCR6 AIRE
301 integumentary system disease 10.4 H2AC18 ERCC6 CD8A CD4 CCR6
302 brain glioma 10.4 H2AC18 CD8A CD4
303 spondyloarthropathy 1 10.4 CD8A CD4 CCR6
304 norwegian scabies 10.4 CD8A CD4
305 omenn syndrome 10.4 H2AC18 CD8A CD4 CCR6 AIRE
306 ovarian serous cystadenocarcinoma 10.4 H2AC18 ERCC6 CD8A
307 hashimoto thyroiditis 10.4 H2AC18 CD8A CD4 CCR6 AIRE
308 orbital cellulitis 10.4 CD8A CD4
309 jejunoileitis 10.4 CD8A CCR6
310 mycobacterium tuberculosis 1 10.4 H2AC18 CD8A CD4 CCR6
311 sensory system disease 10.4 H2AC18 ERCC6 CD4 CCR6
312 acute orbital inflammation 10.4 CD8A CD4
313 exanthem 10.4 H2AC18 CSF3 CD8A CD4 CCR6
314 substance abuse 10.4 H2AC18 CD4 CCR6
315 coronavirus infectious disease 10.4 H2AC18 CSF3 CD8A CD4 CCR6
316 alcohol use disorder 10.4 H2AC18 CD4 CCR6
317 celiac disease 1 10.4 H2AC18 CD8A CD4 CCR6 AIRE
318 thyroid gland disease 10.4 SHBG H2AC18 CD8A CD4 CCR6
319 disorder of sexual development 10.4 SRD5A2 SHBG H2AC18 ERCC6
320 bone marrow cancer 10.4 H2AC18 CSF3 CD8A CD4 CCR6
321 testicular disease 10.4 SHBG H2AC18 ERCC6 CD8A CD4
322 bacterial infectious disease 10.4 H2AC18 CSF3 CD8A CD4 CCR6
323 head and neck cancer 10.4 H2AC18 ERCC6 CD8A CD4 CCR6
324 primary biliary cholangitis 10.4 H2AC18 CD8A CD4 CCR6 AIRE
325 pancytopenia 10.4 H2AC18 CSF3 CD8A CD4
326 lymphatic system cancer 10.4 H2AC18 CD8A CD4 CCR6
327 chromosomal deletion syndrome 10.4 H2AC18 CD4 CCR6
328 viral exanthem 10.4 CD8A CD4
329 behcet syndrome 10.4 H2AC18 CSF3 CD8A CD4 CCR6
330 primary cutaneous t-cell non-hodgkin lymphoma 10.4 H2AC18 CD4 CCR6
331 lymphatic system disease 10.4 H2AC18 CD8A CD4 CCR6
332 tertiary syphilis 10.4 CD8A CD4
333 chancroid 10.4 CD4 CCR6
334 interstitial lung disease 2 10.4 H2AC18 DSP CD8A CD4 CCR6
335 respiratory failure 10.4 H2AC18 CSF3 CD8A CD4 CCR6
336 cerebritis 10.4 CD8A CD4
337 allergic contact dermatitis 10.4 CD8A CD4 CCR6
338 hypotrichosis 2 10.4 LPAR6 LIPH KRT86 KRT83 KRT74 DSG4
339 skin carcinoma 10.4 H2AC18 ERCC6 ERCC3 CD8A CD4 CCR6
340 melanoma, uveal 10.4 H2AC18 ERCC6 CD8A CD4
341 conjunctival squamous cell carcinoma 10.4 KRT15 CD4
342 immune system disease 10.4 H2AC18 CD8A CD4 CCR6
343 respiratory system disease 10.4 H2AC18 ERCC6 CD8A CD4 CCR6
344 metal allergy 10.4 CD8A CD4
345 ectodermal dysplasia 6, hair/nail type 10.4 KRT74 DSG4
346 blood coagulation disease 10.4 H2AC18 ERCC6 CSF3 CD8A CD4 CCR6
347 leukocyte disease 10.4 H2AC18 ERCC6 CSF3 CD8A CD4 CCR6
348 blood platelet disease 10.4 H2AC18 ERCC6 CSF3 CD8A CD4 CCR6
349 ectodermal dysplasia 5, hair/nail type 10.4 KRT74 DSG4
350 microphthalmia, syndromic 6 10.4 SRD5A2 KRT86
351 opportunistic mycosis 10.4 H2AC18 CSF3 CD8A CD4 CCR6 AIRE
352 fungal infectious disease 10.4 H2AC18 CSF3 CD8A CD4 CCR6 AIRE
353 aplastic anemia 10.4 H2AC18 ERCC6 CSF3 CD8A CD4 CCR6
354 hypotrichosis 6 10.4 LPAR6 LIPH KRT86 KRT83 KRT81 KRT74
355 ectodermal dysplasia 4, hair/nail type 10.4 LPAR6 LIPH KRT86 KRT83 KRT81 KRT74
356 severe combined immunodeficiency 10.4 H2AC18 CSF3 CD8A CD4 CCR6 AIRE
357 combined immunodeficiency 10.4 H2AC18 CSF3 CD8A CD4 CCR6 AIRE
358 sickle cell anemia 10.4 H2AC18 CSF3 CD4
359 anti-basement membrane glomerulonephritis 10.4 CD4 CCR6
360 deficiency anemia 10.4 H2AC18 ERCC6 CSF3 CD8A CD4 CCR6
361 peripheral nervous system disease 10.4 H2AC18 ERCC6 CSF3 CD8A CD4 CCR6
362 atrichia with papular lesions 10.4 LPAR6 LIPH KRT86 KRT83 KRT74 H2AC18
363 premature menopause 10.4 SRD5A2 SHBG ERCC6 CD4 AIRE
364 leukemia, chronic myeloid 10.3 H2AC18 CSF3 CD8A CD4 CCR6
365 secondary syphilis 10.3 CD8A CD4
366 leukemia, acute lymphoblastic 10.3 H2AC18 CSF3 CD8A CD4 CCR6
367 leukemia, chronic lymphocytic 10.3 H2AC18 ERCC6 CSF3 CD8A CD4 CCR6
368 gastrointestinal tuberculosis 10.3 CD8A CD4
369 lymphoma, non-hodgkin, familial 10.3 H2AC18 CSF3 CD8A CD4 CCR6
370 sezary's disease 10.3 CD8A CD4 CCR6
371 leukemia, acute myeloid 10.3 H2AC18 ERCC6 CSF3 CD8A CD4 CCR6
372 connective tissue disease 10.3 H2AC18 ERCC6 CSF3 CD8A CD4 CCR6
373 glanders 10.3 CD8A CD4
374 myelodysplastic syndrome 10.3 H2AC18 CSF3 CD8A CD4 CCR6
375 mikulicz disease 10.3 CD4 CCR6
376 immune deficiency disease 10.3 H2AC18 CD8A CD4 CCR6 AIRE
377 adenoid hypertrophy 10.3 CD8A CD4
378 abdominal tuberculosis 10.2 CD8A CD4
379 retinitis pigmentosa 46 10.2 CD8A CD4
380 wilson disease 10.0
381 bladder diverticulum 9.9
382 3-methylglutaconic aciduria, type iii 9.9
383 pili torti, early-onset 9.9
384 hypotonia 9.9
385 body mass index quantitative trait locus 11 9.9 SHBG H2AC18 ERCC6 CD8A CD4 CCR6
386 body dysmorphic disorder 9.9
387 mitochondrial complex iv deficiency, nuclear type 1 9.8
388 cerebral degeneration 9.8
389 cerebellar degeneration 9.8
390 disorder of copper metabolism 9.8
391 mitochondrial disease 9.8
392 cafe-au-lait spots, multiple 9.8
393 popliteal pterygium syndrome 9.8
394 hypertelorism 9.8
395 osseous heteroplasia, progressive 9.8
396 widow's peak 9.8
397 tooth agenesis 9.8
398 hypereosinophilic syndrome 9.8
399 manganese poisoning 9.8
400 hair morphology 2 9.7
401 trichotillomania 9.7
402 alopecia areata 9.7
403 alopecia areata 1 9.7
404 acrodermatitis enteropathica, zinc-deficiency type 9.7
405 argininosuccinic aciduria 9.7
406 trichothiodystrophy 4, nonphotosensitive 9.7
407 netherton syndrome 9.7
408 alopecia, congenital 9.7
409 ectodermal dysplasia 1, hypohidrotic, x-linked 9.7
410 trichothiodystrophy 1, photosensitive 9.7
411 anxiety 9.7
412 alexithymia 9.7
413 covid-19 9.7
414 somatization disorder 9.7
415 acrodermatitis 9.7
416 tinea capitis 9.7
417 folliculitis 9.7
418 pediculus humanus capitis infestation 9.7
419 dermatophytosis 9.7
420 frontal fibrosing alopecia 9.7
421 quinquaud folliculitis decalvans 9.7
422 discoid lupus erythematosus 9.7
423 nephrolithiasis, calcium oxalate 9.7
424 contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a 9.7
425 ataxia-telangiectasia 9.7
426 hypoascorbemia 9.7
427 melanosis, neurocutaneous 9.7
428 ataxia with vitamin e deficiency 9.7
429 woolly hair, hypotrichosis, everted lower lip, and outstanding ears 9.7
430 trichothiodystrophy 9.7
431 leukodystrophy 9.7
432 hydronephrosis 9.7
433 henoch-schoenlein purpura 9.7
434 protein-energy malnutrition 9.7
435 neuronal ceroid lipofuscinosis 9.7
436 early myoclonic encephalopathy 9.7
437 gingival overgrowth 9.7
438 bartter disease 9.7
439 acne 9.7
440 mitochondrial encephalomyopathy 9.7
441 vesicoureteral reflux 9.7
442 cerebral atrophy 9.7

Graphical network of the top 20 diseases related to Hair Disease:



Diseases related to Hair Disease

Symptoms & Phenotypes for Hair Disease

UMLS symptoms related to Hair Disease:


pruritus; exanthema

GenomeRNAi Phenotypes related to Hair Disease according to GeneCards Suite gene sharing:

25 (showing 2, show less)
# Description GenomeRNAi Source Accession Score Top Affiliating Genes
1 no effect GR00402-S-1 10.15 AIRE CCR6 CD4 CD8A CSF3 DSG4
2 no effect GR00402-S-2 10.15 AIRE CCR6 CD4 CSF3 ERCC3 ERCC6

MGI Mouse Phenotypes related to Hair Disease:

45 (showing 1, show less)
# Description MGI Source Accession Score Top Affiliating Genes
1 integument MP:0010771 9.32 CD4 CD8A CSF3 DSG4 DSP ERCC3

Drugs & Therapeutics for Hair Disease

Drugs for Hair Disease (from DrugBank, HMDB, Dgidb, PharmGKB, IUPHAR, NovoSeek, BitterDB):

(showing 18, show less)
# Name Status Phase Clinical Trials Cas Number PubChem Id
1
Eflornithine Approved, Withdrawn Phase 2 70052-12-9 3009
2
Ornithine Approved, Nutraceutical Phase 2 3184-13-2, 70-26-8 6262
3 Anti-Infective Agents Phase 2
4 Antiprotozoal Agents Phase 2
5 Antiparasitic Agents Phase 2
6 Complement System Proteins Phase 1, Phase 2
7 Complement Factor H Phase 1, Phase 2
8 Immunosuppressive Agents Phase 1, Phase 2
9 Immunologic Factors Phase 1, Phase 2
10 Mitogens Phase 1, Phase 2
11
Edetate calcium disodium anhydrous Approved, Vet_approved 62-33-9, 60-00-4 6049
12
Pentetic acid Approved 67-43-6
13
Polidocanol Approved 9002-92-0 78933
14
Petrolatum Approved, Investigational 8009-03-8
15
Cerebrolysin Experimental 12656-61-0
16 Neuroprotective Agents
17 Nootropic Agents
18 Protective Agents

Interventional clinical trials:

(showing 8, show less)
# Name Status NCT ID Phase Drugs
1 Topical Eflornithine Hydrochloride for Pseudofolliculitis Barbae: A Randomized, Double-blinded, Placebo-controlled Trial Unknown status NCT04403282 Phase 4 Eflornithine Topical;Placebo Eflornithine Topical
2 Phase II, Open-Label Study of the Effect of 15% Eflornithine Hydrochloride Cream on Facial Hair of Men of African-American Descent With Pseudofolliculitis Barbae: A Laser Scanning Confocal Microscopy and Video Imaging Study Completed NCT00176995 Phase 2 15% Eflornithine Hdyrochloride
3 Biocellular Regenerative Therapy in Hair Loss: Use of High Density Platelet-Rich Plasma Concentrates and Cell-Enriched Emulsified Adipose-Derived Tissue Stromal Vascular Fraction Enrolling by invitation NCT02849470 Phase 1, Phase 2
4 The Impact of a Pre-Shave Gel and Brush in Males With Pseudofolliculitis Barbae Completed NCT03043534
5 Clinical Safety and Efficacy of Prototype Devices for Hair Growth Control: Task 2.4 Completed NCT00402129
6 Hair Repigmentation in Patients Undergoing on Cerebrolysin Treatment for Neurological Diseases. Completed NCT05288465 Cerebrolysin
7 Tricho-hepato-enteric Syndrome: From Abnormal RNA Decay to Disease Clinical and Biological Characterization of Patients and Collection of Samples -THE-RNA Not yet recruiting NCT04499040
8 Depilatory Cream's Affect on the Occurrence of Pseudofolliculitis Barbae Withdrawn NCT04220502 Early Phase 1 Magic Shave Powder Gold

Search NIH Clinical Center for Hair Disease

Cochrane evidence based reviews: hair diseases

Genetic Tests for Hair Disease

Anatomical Context for Hair Disease

Organs/tissues related to Hair Disease:

FMA: Hair
MalaCards : Skin, Cortex, Brain, Cerebellum, Spinal Cord, Bone Marrow, Thalamus

Publications for Hair Disease

Articles related to Hair Disease:

(showing 383, show less)
# Title Authors PMID Year
1
Transmission electron microscopy of pili annulati. 41
36100477 2022
2
Prevalence and Increase over Time of Twelve Self-reported Skin Symptoms: Data from Two Representative Samples from 1998 and 2015. 41
36172697 2022
3
Paediatric Poliosis as the Presenting Feature of Scalp Vitiligo: A Retrospective Case Series. 41
36200508 2022
4
Case report of a Spanish patient with arrhythmogenic right ventricular cardiomyopathy and palmoplantar keratoderma without plakoglobin and desmoplakin gene modifications. 53 62
17045679 2007
5
A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy. 53 62
9651581 1998
6
Serum Ferritin Levels amongst Individuals with Androgenetic Alopecia in Ile-Ife, Nigeria. 62
36260427 2022
7
The First Evidence of Bacterial Foci in the Hair Part and Dermal Papilla of Scalp Hair Follicles: A Pilot Comparative Study in Alopecia Areata. 62
36233254 2022
8
Exploring the impact of ovariectomy on hair growth: can ovariectomized mouse serve as a model for investigating female pattern hair loss in humans? 62
35486188 2022
9
Hair disorder in dr. Cipto Mangunkusumo cosmetic dermatology and venereology outpatient clinic of Jakarta, Indonesia: A socio-demographic and clinical evaluation. 62
36199901 2022
10
Exploring the effects of Chinese herbal ingredients on the signaling pathway of alopecia and the screening of effective Chinese herbal compounds. 62
35483562 2022
11
Alopecia areata: Recent advances and emerging therapies. 62
35752494 2022
12
Tofacitinib as a pragmatic treatment choice for alopecia areata: A retrospective review. 62
34997820 2022
13
Exome sequencing reveals the first intragenic deletion in ABCA5 underlying autosomal recessive hypertrichosis. 62
35150007 2022
14
Patient-reported long-term outcome following allogeneic hematopoietic stem cell transplantation in pediatric chronic myeloid leukemia. 62
36276159 2022
15
Exosomes Derived from Dermal Papilla Cells Mediate Hair Follicle Stem Cell Proliferation through the Wnt3a/β-Catenin Signaling Pathway. 62
36388171 2022
16
Short communication: Comments on hair disorders associated with dupilumab based on VigiBase. 62
35895603 2022
17
Prevalence of early-onset androgenetic alopecia and its relationship with lifestyle and dietary habits. 62
33913667 2021
18
Alopecias in humans: biology, pathomechanisms and emerging therapies. 62
34431565 2021
19
A novel automated approach to rapid and precise in vivo measurement of hair morphometrics using a smartphone. 62
34251055 2021
20
Evaluation of the level of serum Interleukins (IL-2, IL-4, IL-15 andIL-17) and its relationship with disease severity in patients with alopecia areata. 62
34281739 2021
21
Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies. 62
33988877 2021
22
Clinical and trichoscopic features in various forms of scalp psoriasis. 62
33991148 2021
23
Therapeutic approach with squaric acid dibutylester for steroid resistant-alopecia areata incognita: A pilot study of a single center. 62
34390608 2021
24
Short anagen syndrome: A case series and algorithm for diagnosis. 62
34409646 2021
25
Quality of life measurement in alopecia areata. Position statement of the European Academy of Dermatology and Venereology Task Force on Quality of Life and Patient Oriented Outcomes. 62
34107093 2021
26
Accuracy of clinical diagnosis and videodermoscopy in female pattern hair loss. 62
33141980 2021
27
From Buns to Braids and Ponytails: Entering a New Era of Female Military Hair-Grooming Standards. 62
34397355 2021
28
Phytochemical constituents, distributions and traditional usages of Arnebia euchroma: A review. 62
33524510 2021
29
Association Between Vitamin D and Zinc Levels With Alopecia Areata Phenotypes at a Tertiary Care Center. 62
34079683 2021
30
The role of sleep in telogen effluvium and trichodynia: A commentary in the context of the current pandemic. 62
33387387 2021
31
How good is artificial intelligence (AI) at solving hairy problems? A review of AI applications in hair restoration and hair disorders. 62
33496058 2021
32
Trichotillomania Incognito: Two Case Reports and Literature Review. 62
33796560 2021
33
Loose anagen syndrome in one identical twin girl. 62
33818982 2021
34
Circle Hairs in a Patient with Multiple Myeloma. 62
34848987 2021
35
Defining microRNA signatures of hair follicular stem and progenitor cells in healthy and androgenic alopecia patients. 62
33183906 2021
36
Demographic and Clinical Features of 1,641 Patients with Alopecia Areata, Alopecia Totalis, and Alopecia Universalis: A Single-Center Retrospective Study. 62
33614711 2021
37
The Role of Trichoscopy in Keratosis Follicularis Spinulosa Decalvans: Case Report and Review of the Literature. 62
33614716 2021
38
Assessment of treatment efficacy of diphenylcyclopropenone (DPCP) for alopecia areata 62
31655499 2020
39
Heterogeneity in amount of growth factors secreted by platelets in platelet-rich plasma samples from alopecia patients. 62
32748436 2020
40
Lgr4 Deletion Delays the Hair Cycle and Inhibits the Activation of Hair Follicle Stem Cells. 62
32035093 2020
41
Molecular Modeling of Pathogenic Mutations in the Keratin 1B Domain. 62
32927888 2020
42
Congenital Hair Anomaly in Association with Hypodontia of Permanent Teeth: A Quiz. 62
32619014 2020
43
A randomized, single-blinded, vehicle-controlled study of a topical active blend in the treatment of androgenetic alopecia. 62
32473084 2020
44
Psychometric properties of the updated EORTC module for assessing quality of life in patients with lung cancer (QLQ-LC29): an international, observational field study. 62
32213338 2020
45
Trachyonychia: a retrospective study of 122 patients in a period of 30 years. 62
31923322 2020
46
Female Androgenetic Alopecia: An Update on Diagnosis and Management. 62
31677111 2020
47
A comparative study between submandibular-facial artery island flaps (including perforator flap) and submental artery perforator flap: A novel flap in oral cavity reconstruction. 62
31669971 2019
48
Topical calcipotriol vs narrowband ultraviolet B in treatment of alopecia areata: a randomized-controlled trial. 62
31236672 2019
49
Alopecia Areata Incognita and Diffuse Alopecia Areata: Clinical, Trichoscopic, Histopathological, and Therapeutic Features of a 5-Year Study. 62
31723460 2019
50
Randomized controlled trial on a PRP-like cosmetic, biomimetic peptides based, for the treatment of alopecia areata. 62
30513014 2019
51
Genetic Hair Disorders: A Review. 62
31332722 2019
52
[A girl with unruly hair]. 62
31305964 2019
53
The effect of scalp cooling on CIA-related quality of life in breast cancer patients: a systematic review. 62
30806923 2019
54
A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy. 62
31341463 2019
55
Dietary Protein Deficit and Deregulated Autophagy: A New Clinico-diagnostic Perspective in Pathogenesis of Early Aging, Skin, and Hair Disorders. 62
30984584 2019
56
Cortexolone 17α-Propionate (Clascoterone) is an Androgen Receptor Antagonist in Dermal Papilla Cells In Vitro 62
30811143 2019
57
Pityriasis amiantacea following bone marrow transplant. 62
30758335 2019
58
Ethnobotanical Study of Indigenous Medicinal Plants of Jazan Region, Saudi Arabia. 62
31275409 2019
59
Study on Hair Distribution in Healthy Males for Hair Restoration Design. 62
30277939 2018
60
Quantification of Hair Follicles in the Scalp in Mexican Mestizo Population. 62
30643777 2018
61
Acquired trichorrhexis nodosa: how to diagnose it? 62
30695984 2018
62
Formulation and Evaluation of Licorice Shampoo in Comparison with Commercial Shampoo. 62
30568378 2018
63
Facial Lichen Planopilaris: A Separate Entity or Not? A Case Series. 62
30386080 2018
64
Quality of life in mild and severe alopecia areata patients. 62
29872683 2018
65
Novel splice site mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review. 62
29464811 2018
66
Somatic sprouts of the Purkinje cells in a patient with multiple system atrophy. 62
29575082 2018
67
Spontaneous retroperitoneal hemorrhage in Menkes disease: A rare case report. 62
29419699 2018
68
5α-Reductase isozymes and aromatase mRNA levels in plucked hair from young women with female pattern hair loss. 62
29185104 2018
69
Parietal scalp is another affected area in female pattern hair loss: an analysis of hair density and hair diameter. 62
29343978 2018
70
Novel mutations in the lipase H gene lead to secretion defects of LIPH in Chinese patients with autosomal recessive woolly hair/hypotrichosis (ARWH/HT). 62
29346610 2017
71
Menkes disease: A rare disorder. 62
28955085 2017
72
Three Cases of Hair Loss Analyzed by the Point of View of the Analytical Psychology. 62
29118523 2017
73
Recessive progressive symmetric erythrokeratoderma results from a homozygous loss-of-function mutation of KRT83 and is allelic with dominant monilethrix. 62
27965375 2017
74
Ataxia telangiectasia, Menkes kinky hair disease and neurocutaneous melanosis. 62
27002302 2017
75
[Psychological consequences of hair loss]. 62
28722460 2017
76
Frontal fibrosing alopecia: reflections and hypotheses on aetiology and pathogenesis. 62
27198858 2016
77
Serum Vitamin D in patients with alopecia areata. 62
27730032 2016
78
A Phase III, Multicenter, Parallel-Design Clinical Trial to Compare the Efficacy and Safety of 5% Minoxidil Foam Versus Vehicle in Women With Female Pattern Hair Loss. 62
27391639 2016
79
Hair Follicle Miniaturization in a Woolly Hair Nevus: A Novel "Root" Perspective for a Mosaic Hair Disorder. 62
26894777 2016
80
Experimental white piedra: a robust approach to ultrastructural analysis, scanning electron microscopy and etiological discoveries. 62
26476093 2016
81
Menkes disease: what a multidisciplinary approach can do. 62
27574440 2016
82
Menkes Kinky Hair Disease. 62
26840692 2016
83
Differential Expression of Proteins Associated with the Hair Follicle Cycle - Proteomics and Bioinformatics Analyses. 62
26752403 2016
84
Case Study: Somatic Sprouts and Halo-Like Amorphous Materials of the Purkinje Cells in Huntington's Disease. 62
25962893 2015
85
Psoriatic alopecia. 62
26202646 2015
86
Increased apoptosis and hypomyelination in cerebral white matter of macular mutant mouse brain. 62
26937406 2015
87
RBM28, a protein deficient in ANE syndrome, regulates hair follicle growth via miR-203 and p63. 62
25939713 2015
88
Owner assessment of pruritus and gastrointestinal signs in apparently healthy dogs with no history of cutaneous or noncutaneous disease. 62
26178605 2015
89
Biology of the hair follicle and mechanisms of nonscarring and scarring alopecia. 62
26176280 2015
90
Novel KRT83 and KRT86 mutations associated with monilethrix. 62
25557232 2015
91
Disease Severity, Quality of Life, and Psychiatric Morbidity in Patients With Psoriasis With Reference to Sociodemographic, Lifestyle, and Clinical Variables: A Prospective, Cross-Sectional Study From Lahore, Pakistan. 62
26644955 2015
92
Androgenetic alopecia: new insights into the pathogenesis and mechanism of hair loss. 62
26339482 2015
93
Acitretin-induced alopecia areata: a case report. 62
25198403 2015
94
Evaluation of hair loss. 62
26370640 2015
95
Hair keratin mutations in tooth enamel increase dental decay risk. 62
25347471 2014
96
The function of zebra stripes. 62
24691390 2014
97
Increased expression of Dkk1 by HR is associated with alteration of hair cycle in hairpoor mice. 62
24447645 2014
98
Cerebellar expression of copper chaperone for superoxide, cytosolic cu/zn-superoxide dismutase, 4-hydroxy-2-nonenal, acrolein and heat shock protein 32 in patients with menkes kinky hair disease: immunohistochemical study. 62
25067875 2014
99
Selective hair therapy: bringing science to the fiction. 62
24387677 2014
100
Primary idiopathic pseudopelade of brocq: five case reports. 62
25114452 2014
101
Evaluation of utility of phenol in alopecia areata. 62
24778526 2013
102
Loose anagen hair syndrome in black-haired Indian children. 62
23937400 2013
103
Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix. 62
23981620 2013
104
Novel Frameshift Mutation in TRPS1 in a Ukrainian Patient with Trichorhinophalangeal Syndrome Type I. 62
24574699 2013
105
[Generalised erythema, scaling and hair anomaly]. 62
23604280 2013
106
The difficult hair loss patient: a particular challenge. 62
24574686 2013
107
Dermatological problems of the puberty. 62
24278071 2013
108
Bone mineral density in patients with alopecia areata treated with long-term intralesional corticosteroids. 62
23377403 2013
109
The basic science of hair biology: what are the causal mechanisms for the disordered hair follicle? 62
23159172 2013
110
Transcriptome profile at different physiological stages reveals potential mode for curly fleece in Chinese tan sheep. 62
23990983 2013
111
Videocapillaroscopic alterations in alopecia areata. 62
24163812 2013
112
Multivariate analysis of prognostic factors in patients with rapidly progressive alopecia areata. 62
23006662 2012
113
Menkes kinky hair syndrome: a case report. 62
23217945 2012
114
Menkes syndrome presenting as possible child abuse. 62
23259200 2012
115
Keratin 71 mutations: from water dogs to woolly hair. 62
22971920 2012
116
A missense mutation within the helix initiation motif of the keratin K71 gene underlies autosomal dominant woolly hair/hypotrichosis. 62
22592156 2012
117
Evaluation of efficacy, safety and effects on symptoms of androgenization of a generic oral contraceptive containing chlormadinone acetate 2 mg/ethinylestradiol 0.03 mg. 62
22445436 2012
118
A study to evaluate the efficacy of various topical treatment modalities for alopecia areata. 62
23766611 2012
119
Menkes kinky hair disease. 62
23112368 2012
120
Pili annulati coincident with alopecia areata, autoimmune thyroid disease, and primary IgA deficiency: case report and considerations on the literature. 62
23275769 2012
121
Lichen planopilaris following hair transplantation and face-lift surgery. 62
21985326 2012
122
Estrogen leads to reversible hair cycle retardation through inducing premature catagen and maintaining telogen. 62
22792225 2012
123
Menkes kinky hair syndrome: a rare neurodegenerative disease. 62
22919529 2012
124
Hair care practices and scalp/hair disease in African American girls. 62
21571179 2011
125
Concomitant manifestation of pili annulati and alopecia areata: coincidental rather than true association. 62
21537827 2011
126
Proteomics demonstration that histone H4 is a colchicine-induced retro-modulator of growth and alkaline phosphatase activity in hair follicle dermal papilla culture. 62
21362507 2011
127
Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families. 62
21188418 2011
128
Pathology, clinical features and treatments of congenital copper metabolic disorders--focus on neurologic aspects. 62
21112168 2011
129
[Control of bone remodeling by nervous system. Diagnosis and treatments for complex regional pain syndrome]. 62
21123940 2010
130
Common dermatologic diseases among students at a tertiary care center in Lebanon. 62
21409941 2010
131
Familial woolly hair disease. 62
20519796 2010
132
Overexpression of Hr links excessive induction of Wnt signaling to Marie Unna hereditary hypotrichosis. 62
19897589 2010
133
Ethics in trichology. 62
21188023 2010
134
Trichothiodystrophy and fragile hair: the distinction between diagnostic signs and diagnostic labels in childhood hair disease. 62
19754869 2009
135
Loose anagen hair syndrome: an unusual cause of alopecia of cosmetic importance only. 62
19735522 2009
136
Founder mutations in the lipase h gene in families with autosomal recessive woolly hair/hypotrichosis. 62
19262606 2009
137
Androgenetic alopecia in males: a histopathological and ultrastructural study. 62
19527330 2009
138
Approach to hair loss in women of color. 62
19608062 2009
139
Analysis of dermatologic events in patients with cancer treated with lapatinib. 62
18600445 2009
140
Proliferation, DNA repair and apoptosis in androgenetic alopecia. 62
18702626 2009
141
Menkes kinky hair disease: A case report. 62
18801184 2008
142
Pseudopelade of Brocq. 62
18715295 2008
143
Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3). 62
18461368 2008
144
Cutaneous and mucosal manifestations in patients on maintenance hemodialysis: a study of 101 patients in Sari, Iran. 62
19377214 2008
145
Evaluation of new measures of the impact of hypothyroidism on quality of life and symptoms: the ThyDQoL and ThySRQ. 62
18380641 2008
146
Healthy hair: what is it? 62
18004288 2007
147
Adding HCV treatment to HIV treatment in HIV-HCV coinfected patients: the impact on the different dimensions of fatigue and self-reported side effects. 62
17616331 2007
148
Reversible alopecia universalis secondary to PEG-interferon alpha-2b and ribavirin combination therapy in a patient with chronic hepatitis C virus infection. 62
17700271 2007
149
[The use of lamotrigine in female patients]. 62
16523355 2007
150
Scalp and hair problems. 62
17784666 2007
151
Menkes syndrome presenting as myoclonic seizures: neuroimaging and EEG observations. 62
17621528 2007
152
Patient-reported complications and functional outcomes of male-to-female sex reassignment surgery. 62
17109225 2006
153
Menkes kinky hair disease (Menkes syndrome). A case report. 62
17053847 2006
154
Immunoreactivity of corticotropin-releasing hormone, adrenocorticotropic hormone and alpha-melanocyte-stimulating hormone in alopecia areata. 62
16761960 2006
155
More than one gene involved in monilethrix: intracellular but also extracellular players. 62
16702971 2006
156
Antiandrogen therapy for skin and hair disease. 62
16677962 2006
157
Androgenetic alopecia: stress of discovery. 62
16673981 2006
158
User experience with an oral contraceptive containing ethinylestradiol 30mug and drospirenone 3mg (yasmin((r))) in clinical practice. 62
16879004 2006
159
Female pattern hair loss, sebum excretion and the end-organ response to androgens. 62
16403099 2006
160
Female pattern hair loss and its relationship to permanent/cicatricial alopecia: a new perspective. 62
16382668 2005
161
Autopsy case of acute encephalopathy linked to familial hemiplegic migraine with cerebellar atrophy and mental retardation. 62
16193840 2005
162
Psychological aspects of hair disease. 62
17166214 2005
163
Pili trianguli et canaliculi is a defect of inner root sheath keratinization: ultrastructural observations of anomalous tonofilament organization in a case. 62
15900128 2005
164
Human hair abnormalities resulting from inherited desmosome gene mutations. 62
16077256 2005
165
Trichotemnomania: obsessive-compulsive habit of cutting or shaving the hair. 62
15627101 2005
166
Alopecia areata universalis sparing nevus flammeus. 62
15785052 2005
167
[Alopecia areata and treatment]. 62
15516057 2004
168
Differential diagnosis of hair loss in children. 62
16281597 2004
169
Effect of estrogen on plasma ceruloplasmin level in rats exposed to acute stress. 62
15122050 2004
170
An unusual Ala12Thr polymorphism in the 1A alpha-helical segment of the companion layer-specific keratin K6hf: evidence for a risk factor in the etiology of the common hair disorder pseudofolliculitis barbae. 62
15086549 2004
171
Restoration of hair growth with topical diphencyprone in mouse and rat models of alopecia areata. 62
14639378 2003
172
Patient sources of drug information and attitudes to their provision: a corticosteroid model. 62
14584224 2003
173
[New and established methods in therapy of hair diseases]. 62
12942187 2003
174
Hair colouring, permanent styling and hair structure. 62
17163926 2003
175
Morphological approach to hair disorders. 62
12894995 2003
176
Renal transplant recipient attitudes toward steroid use and steroid withdrawal. 62
12709080 2003
177
Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix. 62
12653715 2003
178
Recurrent E413K mutation of hHb6 in a Japanese family with monilethrix. 62
12771477 2003
179
[Visual field defect in a patient given sodium valporate then carbamazepine: possible effect of aminotransferase inhibition]. 62
11984493 2002
180
Hair and systemic disease. 62
11705356 2001
181
Scarring alopecia and the dermatopathologist. 62
11437938 2001
182
HLA-A2 restricted, melanocyte-specific CD8(+) T lymphocytes detected in vitiligo patients are related to disease activity and are predominantly directed against MelanA/MART1. 62
11407977 2001
183
A case of folliculitis decalvans involving the beard, face and nape. 62
11476113 2001
184
[Is alopecia areata a psychosomatic disease?]. 62
11270270 2001
185
[Loose anagen hair syndrome: a familial case with fetal hair in meconium]. 62
11226903 2001
186
Is kinky-hair disease a misnomer for Menkes syndrome? 62
11176670 2001
187
Mitochondrial encephalomyopathy with lactic acidosis and stroke like episodes (MELAS) with prominent degeneration of the intestinal wall and cactus-like cerebellar pathology. 62
11078225 2000
188
Cathepsin L deficiency as molecular defect of furless: hyperproliferation of keratinocytes and pertubation of hair follicle cycling. 62
11023992 2000
189
[Interrelations between physician, hairdresser and mass media in management of hair loss]. 62
11153357 2000
190
Pseudopelade of Brocq in beard area. 62
10767699 2000
191
[Plica polonica in the 21st century]. 62
10789085 2000
192
Nucleotide excision repair and human syndromes. 62
10688865 2000
193
Menkes kinky hair disease: an unusual case. 62
10872109 2000
194
Matting of hair: a multifactorial enigma. 62
11053910 2000
195
The presence of loose anagen hairs obtained by hair pull in the normal population. 62
10674377 1999
196
Two different mutations in the same codon of a type II hair keratin (hHb6) in patients with monilethrix. 62
10594761 1999
197
Dermatopathology of common hair problems. 62
11749884 1999
198
Prenatal sonographic diagnosis of Aarskog syndrome. 62
10511304 1999
199
Netherton's syndrome: increased likelihood of diagnosis by examining eyebrow hairs. 62
10583065 1999
200
Monilethrix: a novel mutation (Glu402Lys) in the helix termination motif and the first causative mutation (Asn114Asp) in the helix initiation motif of the type II hair keratin hHb6. 62
10469314 1999
201
Monilethrix--improvement by hormonal influences? 62
10469416 1999
202
[Androgenetic alopecia, hirsutism and hypertrichosis]. 62
10330884 1999
203
Molecular and functional aspects of the hairless (hr) gene in laboratory rodents and humans. 62
9832313 1998
204
A variable monilethrix phenotype associated with a novel mutation, Glu402Lys, in the helix termination motif of the type II hair keratin hHb1. 62
9665406 1998
205
Hair today, gone tomorrow: transgenic mice with human repair deficient hair disease. 62
9657142 1998
206
[Rare hyperimmunoglobulinemia E syndromes]. 62
9775139 1998
207
Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality. 62
9426063 1998
208
Topical liposome targeting of dyes, melanins, genes, and proteins selectively to hair follicles. 62
9588863 1998
209
A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix. 62
9402962 1997
210
Increased scalp skin and serum 5 alpha-reductase reduced androgens in a man relevant to the acquired progressive kinky hair disorder and developing androgenetic alopecia. 62
9301590 1997
211
Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix. 62
9241275 1997
212
Side effects of adjuvant chemotherapy: perceptions of node-negative breast cancer patients. 62
9205966 1997
213
Urologic abnormalities in Menkes' kinky hair disease: report of three cases. 62
9165480 1997
214
Menkes' kinky hair disease associated with a large bladder diverticulum: a case report. 62
9255676 1997
215
Topical liposome delivery of molecules to hair follicles in mice. 62
9039973 1997
216
Hair problems in women. 62
9034660 1997
217
Effects of interleukins, colony-stimulating factor and tumour necrosis factor on human hair follicle growth in vitro: a possible role for interleukin-1 and tumour necrosis factor-alpha in alopecia areata. 62
8977716 1996
218
Human keratin diseases: hereditary fragility of specific epithelial tissues. 62
9028791 1996
219
Menkes' Kinky Hair disease: new considerations. 62
9141833 1996
220
Kinky hair disease with multiple eruption cysts: a case report. 62
8936518 1996
221
Skin disorders in black children. 62
8954271 1996
222
Pili bifurcati: occurring in association with the mosaic trisomy 8 syndrome. 62
8818460 1996
223
Investigation of structural proteins in human hair defects using anagen follicles. 62
8776364 1996
224
Linkage of monilethrix to the trichocyte and epithelial keratin gene cluster on 12q11-q13. 62
8618025 1996
225
Brittle and sparse hair with normal cystine content caused by methionine deficiency? 62
8721497 1996
226
A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13. 62
8634717 1995
227
Helical hairs: a new hair anomaly in a patient with Netherton's syndrome. 62
7648886 1995
228
Menkes' kinky-hair disease: radiologic findings in a patient treated with copper histidinate. 62
7704673 1995
229
[The morphological signs of hair disease in children poisoned by thallium and boron]. 62
7638883 1995
230
Unusual association of juvenile macular dystrophy with congenital hypotrichosis: occurrence in two siblings suggesting autosomal recessive inheritance. 62
7648037 1995
231
Primary osteoma cutis--multiple café-au-lait spots and woolly hair anomaly. 62
7761159 1995
232
Nucleotide excision repair syndromes: molecular basis and clinical symptoms. 62
7746858 1995
233
Cerebellar superoxide dismutase expression in Menkes' kinky hair disease: an immunohistochemical investigation. 62
7484097 1995
234
Does interleukin-1 induce hair loss? 62
8573920 1995
235
[Menkes disease]. 62
7845659 1994
236
[Menkes' kinky hair disease: a clinical and pathological case report with special reference to glial changes in the brain damage]. 62
7826987 1994
237
Contraception with NORPLANT implants. 62
7844209 1994
238
Menkes kinky hair disease. 62
8028455 1994
239
Electrophysiological and 99mTc-HMPAO-SPECT studies in Menkes disease. 62
7943608 1994
240
Histochemical study of mitochondrial enzymes in cerebellar cortex of macular mutant mouse, a model of Menkes kinky hair disease. 62
8009964 1994
241
Copper distribution in fetus and placenta of the macular mutant mouse as a model of Menkes kinky hair disease. 62
7873696 1994
242
A new clinical disorder of twisted and rolled body hairs with multiple, large knots. 62
8277027 1994
243
Cytokeratin expression in alopecia areata hair follicles. 62
7511864 1994
244
Quality of life and maladjustment associated with hair loss in women with alopecia androgenetica. 62
8146707 1994
245
Effect of age and sex on copper-induced toxicity in the macular mutant mouse. An animal model for Menkes' kinky-hair disease. 62
7509170 1993
246
Cytochrome C oxidase deficiency and neuronal involvement in Menkes' kinky hair disease: immunohistochemical study. 62
8293191 1993
247
[Trichomegaly in HIV infection]. 62
8259476 1993
248
Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F. 62
8253091 1993
249
Menkes kinky hair disease: characteristic MR angiographic findings. 62
8237696 1993
250
Evidence for serum factors modulating antibody production in normal and macular mice. 62
8364504 1993
251
Nucleotide excision repair. II: From yeast to mammals. 62
8337762 1993
252
Intracellular distribution of hepatic copper in macular mutant mice. An animal model of Menkes' kinky-hair disease. 62
7688531 1993
253
Recovery of decreased antibody production by ceruloplasmin in the macular mutant mouse. 62
8488341 1993
254
Neuropathological study on cerebellum of macular mutant mouse heterozygote. 62
8310789 1993
255
The decreased immune responses in macular mouse, a model of Menkes' kinky hair disease. 62
8434133 1993
256
'Kinky hair' disease sheds light on copper metabolism. 62
8490649 1993
257
Urate oxidase activity and copper content in the liver of macular mutant mouse, a model animal for human congenital copper deficiency, Menkes' kinky hair disease. 62
1819648 1991
258
Psychological characteristics of women with androgenetic alopecia: a controlled study. 62
1911317 1991
259
Copper-induced toxicity in macular mutant mouse: an animal model for Menkes' kinky-hair disease. 62
1871775 1991
260
Disorders of the hair and scalp in children. 62
1870910 1991
261
Correction of cerebrospinal fluid copper in Menkes kinky hair disease. 62
1930426 1991
262
Movement disorder with abnormal copper metabolism--a case report and review of the literature. 62
1942656 1991
263
[A case of Menkes' kinky hair disease with a renal calculus and diverticula of the bladder]. 62
1908921 1991
264
MR of progressive neurodegenerative change in treated Menkes' kinky hair disease. 62
2046911 1991
265
Menkes' kinky hair disease: morphological and immunohistochemical comparison of two autopsied patients. 62
2028748 1991
266
Metallothionein messenger RNA levels in the macular mutant mouse: an animal model of Menkes' kinky-hair disease. 62
1912099 1991
267
[Acceptance and subjective well-being with a norgestimate combination pill]. 62
1916521 1991
268
Hair casts. 62
2050233 1991
269
[A pathophysiological study of macular mutant mouse as a model of human Menkes kinky hair disease. I. Copper contents and copper dependent enzyme activities in various organs]. 62
2175632 1990
270
[A pathophysiological study of macular mutant mouse as a model of human Menkes kinky hair disease. II. Analysis of brain metabolism using 31P- and 1H-nuclear magnetic resonance spectroscopy]. 62
2261231 1990
271
[Menkes' kinky hair disease: report of 2 cases]. 62
2178069 1990
272
D-penicillamine-induced copper deficiency in suckling mice: neurological abnormalities and brain mitochondrial enzyme activities. 62
2170057 1990
273
Matting of scalp hair during shampooing--a new look. 62
2347105 1990
274
Electron microscopic study on the homozygote (Ml/Ml) of the macular mutant mouse. 62
2288383 1990
275
A comparative immunocytochemical study of human cerebellar cortex in X-chromosome-linked copper malabsorption (Menkes' kinky hair disease) and granule cell type cerebellar degeneration. 62
2511498 1989
276
Menkes' Disease (kinky Hair Disease). 62
28128144 1989
277
Why men with hair loss go to the doctor. 62
2675157 1989
278
Manganese in scalp hair: problems of exogenous manganese and implications for manganese monitoring in Groote Eylandt Aborigines. 62
2781270 1989
279
[Menkes' kinky hair disease: report of one case]. 62
2637598 1989
280
Cerebral MR of Menkes kinky-hair disease. 62
2492723 1989
281
Decreased blood flow and oxygen metabolism in the cerebellum, brain stem and thalamus in a case with Menkes kinky hair disease. 62
2618967 1989
282
Golgi study on the homozygote (Ml/Ml) of macular mutant mouse. 62
2473662 1989
283
Menkes kinky hair disease with 'ragged red' fibers. 62
3234609 1988
284
Atypical Menkes steely hair disease. 62
3189407 1988
285
Atypical form of Menkes kinky hair disease with mitochondrial NADH-CoQ reductase deficiency. 62
2452375 1988
286
Copper metabolism in the macular mutant mouse: an animal model of Menkes's kinky-hair disease. 62
3219371 1988
287
Biochemical study on the brain of the macular mutant mouse as a model of Menkes' kinky hair disease. 62
2453126 1988
288
Golgi study on macular mutant mouse after copper therapy. 62
2462325 1988
289
Kinky hair disease: twenty five years later. 62
2839049 1988
290
Catecholamine metabolism in kinky hair disease. 62
3233105 1988
291
Electron microscopic study on brain of macular mutant mouse after copper therapy. 62
3201920 1988
292
[Hair disease or the effect of heat (fire)?]. 62
3407335 1988
293
Hair bands in facio-genito-popliteal syndrome. A never before described hair anomaly. 62
3444788 1987
294
[Alopecia areata in children]. 62
3686512 1987
295
Diagnostic techniques for hair disorders. Part II: Microscopic examination of hair bulbs, tips, and casts. 62
3677794 1987
296
Diagnostic techniques for hair disorders. Part I: Microscopic examination of the hair shaft. 62
3652734 1987
297
Structural abnormalities of the hair shaft. 62
3805378 1987
298
Light and electron microscopic study on cerebellar cortex of macular mutant mouse as a model of Menkes kinky hair disease. 62
2821841 1987
299
Golgi study on brain of macular mutant mouse as a model of Menkes kinky hair disease. 62
3577690 1987
300
Metallothionein in kidney and liver of the macular mouse as an animal model of Menkes' kinky hair disease. 62
3449862 1987
301
Clinico-pathological study on macular mutant mouse. 62
3564905 1987
302
Neuronal and vascular disorders of the brain and spinal cord in Menkes kinky hair disease. 62
3130871 1987
303
Abnormal copper metabolism and regulation of metallothionein gene expression in Menkes' disease. 62
2959538 1987
304
Cerebral lipid and protein abnormalities in Menkes' steely-hair disease. 62
3599492 1986
305
Severely deficient binding of 1,25-dihydroxyvitamin D to its receptors in a patient responsive to high doses of this hormone. 62
3011841 1986
306
Catecholamine metabolism in steely hair disease. 62
2941501 1986
307
[An autopsy case of Menkes' kinky hair disease--pathological and biochemical studies on the central nervous system]. 62
3707768 1986
308
Menkes steely hair disease. 62
3721573 1986
309
Cerebellar changes of the female mice heterozygous for brindled gene. 62
3962601 1986
310
Thalamic lesions in a patient with Menkes kinky-hair disease. 62
4064386 1985
311
[Menkes syndrome with excessive skeletal changes]. 62
2996077 1985
312
Menkes' kinky hair disease: clinical and experimental study. 62
4042823 1985
313
Structural changes of hair after incorporation of the proline analogue L-azetidine-2-carboxylic acid. A model of hair disease by alteration of primary structure. 62
2408388 1985
314
Abnormalities of Purkinje cell arborization in brindled mouse cerebellum. A Golgi study. 62
4038413 1985
315
Kinky hair disease with suspected pseudo-Bartter syndrome. 62
4061786 1985
316
Neuropathologic study in the heterozygotes of X-linked brindled mutant mouse. 62
4050346 1985
317
[CT findings in Menkes' kinky hair disease]. 62
6712844 1984
318
Autoradiographic demonstration of the copper-accumulating tissues in mice with a defect homologous to Menkes' Kinky Hair disease. 62
6417634 1983
319
Copper-binding proteins in the liver and kidney from the patients with Menkes' kinky hair disease. 62
6836561 1983
320
[Menkes' kinky hair disease: report of a case]. 62
6821602 1983
321
Mitochondrial abnormalities in Menkes' kinky hair disease (MKHD). Electron-microscopic study of the brain from an autopsy case. 62
6868958 1983
322
Cytochrome c oxidase deficiency in Menkes kinky hair disease. 62
6322607 1983
323
Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphism. 62
6576980 1983
324
Histochemical studies of fibroblasts from patients with Menkes kinky hair disease and Wilson's disease. 62
6290431 1982
325
Prenatal and postnatal diagnosis of diseases of copper metabolism. 62
6753725 1982
326
A defect in catecholamine metabolism in kinky-hair disease. 62
7137961 1982
327
[A syndrome: uncombable hair. Observation of 6 members of a family with pili canaliculi, associated with pili torti, progressive alopecia, atopic eczema and hamartomas]. 62
7107281 1982
328
[Neuropathological study of Menkes' kinky hair disease: on the mechanism of development of cerebrovascular lesions (author's transl)]. 62
7093069 1982
329
A new rat mutant with defective overhairs and spongy degeneration of the central nervous system: clinical and pathologic studies. 62
7078076 1982
330
Menkes' kinky hair disease. I. Comparison of classical and unusual clinical and biochemical features in two patients. 62
7091567 1982
331
Menkes' kinky hair disease. II. A clinicopathological report of three cases. 62
7091568 1982
332
Menkes' kinky hair disease. 62
7187623 1982
333
Tissue copper concentrations of patients with Menke's kinky hair disease. 62
7211802 1981
334
[Spun glass hair (author's transl)]. 62
7271317 1981
335
Diagnosis of hair disease. 62
7232277 1980
336
[Trichopoliodystrophy or Menkes disease]. 62
7002275 1980
337
Polyamine metabolism in Menkes kinky hair disease. 62
6772349 1980
338
Copper and neurological function. 62
6907087 1980
339
Distribution of ingested and injected radiocopper in two patients with Menkes' kinky hair disease. 62
514694 1979
340
Kinky hair disease. Biochemical, histochemical, and ultrastructural studies. 62
514687 1979
341
Thalamic degeneration in X-chromosome--linked copper malabsorption. 62
443770 1979
342
Inducibility of metallothionein biosynthesis in cultured normal and Menkes kinky hair disease fibroblasts: effects of copper and cadmium. 62
471576 1979
343
[Autopsy case of Menkes kinky hair disease]. 62
439455 1979
344
Management of hair problems. 62
370041 1979
345
Failure of human milk therapy in Menkes' kinky hair disease. 62
581719 1979
346
Kinky hair disease. Report of a case. 62
282544 1978
347
Menkes' syndrome (kinky hair disease) [proceedings]. 62
718236 1978
348
[Connective tissue diseases with cutaneous manifestation (author's transl)]. 62
754606 1978
349
Cell culture studies of Menkes kinky hair disease. 62
699339 1978
350
Metal-binding studies of metallothioneins in Menkes kinky hair disease. 62
699318 1978
351
An autopsy case of Menkes kinky hair disease. 62
716884 1978
352
Menkes' disease: neurophysiological aspects. 62
97372 1978
353
[Kinky hair disease (Menkes' syndrome)]. 62
691373 1978
354
[Menkes' disease (new skin and hair ultrastructural abnormalities) (author's transl)]. 62
707942 1978
355
Menkes kinky-hair disease. A report on its pathology. 62
654875 1978
356
New screening method for Wilson's disease and Menkes' kinky-hair disease. 62
73055 1977
357
Menkes' kinky (steely) hair disease. 62
588193 1977
358
Menkes' kinky hair disease. 62
865681 1977
359
[Menkes' kinky hair disease--2 cases]. 62
558778 1977
360
The peroxisomes of human hepatocytes. 62
190476 1977
361
Fine structure of the cerebellar cortex in Menkes Kinky-hair disease. X-chromosome-linked copper malabsorption. 62
831687 1977
362
Copper incorporation studies on cultured cells for prenatal diagnosis of Menkes' disease. 62
58201 1976
363
Inborn errors of copper metabolism: kinky hair disease and hepatolenticular degeneration. Therapeutic approaches. 62
979354 1976
364
Menkes' kinky hair disease: a light and electron microscopic study of the eye. 62
1245386 1976
365
Fine structural changes in the cerebellar cortex in kinky hair disease. 62
1028277 1976
366
Kinky hair disease. Study of copper metabolism with use of 67Cu. 62
1180729 1975
367
[A patient with kinky hair disease (Menke's disease)]. 62
1168863 1975
368
Letter: Menkes' kinky hair disease treated with subcutaneous copper sulphate. 62
4140440 1974
369
Neuropathologic aspects in Menkes' Kinky hair disease (trichopoliodystrophy). Menkes' Kinky hair disease. 62
4140481 1974
370
Copper deficiency in the developing rat brain: a possible model for Menkes' steely-hair disease. 62
4368537 1974
371
Menkes kinky hair disease. A defect in metallothionein metabolism? 62
4458824 1974
372
Study of copper metabolism in kinky hair disease (Menkes' disease) and in hepatolenticular degeneration (Wilson's disease) utilizing 67Cu and radioactivity counting in the total body and various tissues. 62
4219083 1974
373
Widow's peak scalp-hair anomaly and its relation to ocular hypertelorism. 62
4128017 1973
374
[Kinky hair disease--a new syndrome with cerebral degeneration]. 62
4588328 1973
375
A previously undescribed hereditary hair anomaly (pseudo-monilethrix). 62
4726892 1973
376
Menkes' steely-hair (kinky-hair) disease. 62
4123446 1973
377
Menkes' kinky hair disease: further definition of the defect in copper transport. 62
4120259 1973
378
Kinky hair disease. 62
5045346 1972
379
The ocular pathology of Menkes' disease. (Kinky hair disease). 62
5699324 1968
380
Kinky hair disease. II. Biochemical studies. 62
5922551 1966
381
Kinky hair disease. I. Clinical and pathological features. 62
5922550 1966
382
[Local thallium ointment therapy of mycotic hair disease of the skull; preliminary communication]. 62
14378319 1954
383
[Hemiatrophia faciei sinistra with hair anomaly and numerous abnormalities]. 62
13033487 1952

Variations for Hair Disease

Expression for Hair Disease

Search GEO for disease gene expression data for Hair Disease.

Pathways for Hair Disease

Pathways related to Hair Disease according to GeneCards Suite gene sharing:

(showing 2, show less)
# Super pathways Score Top Affiliating Genes
1
Show member pathways
11.71 KRT86 KRT83 KRT81 KRT74 KRT15 DSP
2 11.03 CD8A CD4 CCR6

GO Terms for Hair Disease

Cellular components related to Hair Disease according to GeneCards Suite gene sharing:

(showing 2, show less)
# Name GO ID Score Top Affiliating Genes
1 keratin filament GO:0045095 9.56 KRT86 KRT83 KRT81 KRT74
2 intermediate filament GO:0005882 9.23 KRT86 KRT83 KRT81 KRT74 KRT15 DSP

Biological processes related to Hair Disease according to GeneCards Suite gene sharing:

(showing 2, show less)
# Name GO ID Score Top Affiliating Genes
1 keratinization GO:0031424 9.56 KRT86 KRT83 KRT81 KRT74
2 intermediate filament organization GO:0045109 9.4 KRT86 KRT83 KRT81 KRT74 KRT15 DSP

Molecular functions related to Hair Disease according to GeneCards Suite gene sharing:

(showing 1, show less)
# Name GO ID Score Top Affiliating Genes
1 structural constituent of skin epidermis GO:0030280 9.23 KRT86 KRT83 KRT81 KRT74

Sources for Hair Disease

2 CDC
6 CNVD
8 Cosmic
9 dbSNP
10 DGIdb
16 EFO
17 ExPASy
18 FMA
19 GARD
27 GO
28 GTR
29 HMDB
30 HPO
31 ICD10
32 ICD10 via Orphanet
33 ICD11
34 ICD9CM
35 IUPHAR
36 LifeMap
38 LOVD
40 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
52 NINDS
53 Novoseek
55 ODiseA
56 OMIM via Orphanet
57 OMIM® (Updated 08-Dec-2022)
61 PubChem
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 Tocris
71 UMLS
72 UMLS via Orphanet
Content
Loading form....