MCID: ACH007
MIFTS: 22

Achenbach Syndrome

Categories: Blood diseases, Skin diseases

Aliases & Classifications for Achenbach Syndrome

MalaCards integrated aliases for Achenbach Syndrome:

Name: Achenbach Syndrome 12 15 17
Paroxysmal Hematoma of the Finger 12

Classifications:



External Ids:

Disease Ontology 12 DOID:6687
NCIt 49 C35467
SNOMED-CT 67 238824006
UMLS 71 C0473563

Summaries for Achenbach Syndrome

MalaCards based summary : Achenbach Syndrome, also known as paroxysmal hematoma of the finger, is related to cyanosis, transient neonatal and critical illness polyneuropathy. An important gene associated with Achenbach Syndrome is F3 (Coagulation Factor III, Tissue Factor), and among its related pathways/superpathways are Formation of Fibrin Clot (Clotting Cascade) and Complement and coagulation cascades. Affiliated tissues include skin.

Wikipedia : 74 Paroxysmal hand hematoma is a skin condition characterized by spontaneous focal hemorrhage into the palm... more...

Related Diseases for Achenbach Syndrome

Diseases related to Achenbach Syndrome via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 208, show less)
# Related Disease Score Top Affiliating Genes
1 cyanosis, transient neonatal 10.1
2 critical illness polyneuropathy 10.0 F3 CRP
3 aspiration pneumonitis 10.0 F3 CRP
4 hantavirus hemorrhagic fever with renal syndrome 10.0 F3 CRP
5 multicentric castleman disease 10.0 F3 CRP
6 autoimmune disease of blood 10.0 F3 CRP
7 mycoplasma pneumoniae pneumonia 10.0 F3 CRP
8 angina pectoris 10.0 F3 CRP
9 scrub typhus 10.0 F3 CRP
10 intermediate coronary syndrome 10.0 F3 CRP
11 pyoderma 10.0 F3 CRP
12 carotid artery disease 9.9 F3 CRP
13 peripheral artery disease 9.9 F3 CRP
14 endocarditis 9.9 F2 CRP
15 orbital osteomyelitis 9.9 F2 CRP
16 small intestine diverticulitis 9.9 F2 CRP
17 hematocele of tunica vaginalis testis 9.9 F2 CRP
18 ascending cholangitis 9.9 F2 CRP
19 intracranial berry aneurysm 9.9 F3 CRP
20 splenic abscess 9.9 F2 CRP
21 acalculous cholecystitis 9.9 F2 CRP
22 cholesterol embolism 9.9 F2 CRP
23 abducens nerve disease 9.9 F2 CRP
24 branch retinal artery occlusion 9.9 F2 CRP
25 retinal artery occlusion 9.9 F2 CRP
26 acute cholangitis 9.9 F2 CRP
27 mastoiditis 9.9 F2 CRP
28 abdominal tuberculosis 9.9 F2 CRP
29 paralytic ileus 9.9 F2 CRP
30 ileus 9.9 F2 CRP
31 common bile duct disease 9.9 F2 CRP
32 bile duct disease 9.9 F2 CRP
33 pyuria 9.9 F2 CRP
34 toxic shock syndrome 9.9 F3 CRP
35 central retinal artery occlusion 9.9 F2 CRP
36 kwashiorkor 9.9 F2 CRP
37 pleural empyema 9.9 F2 CRP
38 hemorrhoid 9.9 F2 CRP
39 ischemic colitis 9.8 F2 CRP
40 retinal vascular occlusion 9.8 F2 CRP
41 choledocholithiasis 9.8 F2 CRP
42 plasma protein metabolism disease 9.8 F2 CRP
43 mitral valve insufficiency 9.8 F2 CRP
44 chronic venous insufficiency 9.8 F2 CRP
45 venous insufficiency 9.8 F2 CRP
46 portal vein thrombosis 9.8 F2 CRP
47 fournier gangrene 9.8 F3 F2
48 leptospirosis 9.8 F2 CRP
49 papillary adenofibroma 9.8 F3 F2
50 femoral neuropathy 9.8 F3 F2
51 lateral sinus thrombosis 9.8 F3 F2
52 giant hemangioma 9.8 F3 F2
53 hemangioma 9.8 F3 F2
54 dic in newborn 9.8 F3 F2
55 waterhouse-friderichsen syndrome 9.8 F3 F2
56 hemopneumothorax 9.8 F3 F2
57 syphilis 9.8 F2 CRP
58 gastric hemangioma 9.8 F3 F2
59 hepatic infarction 9.8 F3 F2
60 intermittent claudication 9.8 F2 CRP
61 qualitative platelet defect 9.8 F3 F2
62 hemopericardium 9.8 F3 F2
63 cerebral sinovenous thrombosis 9.8 F3 F2
64 prothrombin deficiency 9.8 F3 F2
65 infective endocarditis 9.8 F2 CRP
66 acute cystitis 9.8 F2 CRP
67 sagittal sinus thrombosis 9.8 F3 F2
68 autoimmune disease of gastrointestinal tract 9.8 F2 CRP
69 cerebral falx meningioma 9.8 F3 F2
70 intracranial hypotension 9.8 F3 F2
71 splenic sequestration 9.8 F3 F2
72 obstructive jaundice 9.8 F2 CRP
73 hepatic coma 9.8 F3 F2
74 nonarteritic anterior ischemic optic neuropathy 9.8 F2 CRP
75 acute hemorrhagic encephalitis 9.8 F3 F2
76 alpha-2-plasmin inhibitor deficiency 9.8 F3 F2
77 vitamin k deficiency bleeding 9.8 F3 F2
78 hantavirus pulmonary syndrome 9.8 F3 F2
79 hemarthrosis 9.8 F3 F2
80 intracranial hypertension, idiopathic 9.8 F3 F2
81 intracranial hypertension 9.8 F3 F2
82 thrombasthenia 9.8 F3 F2
83 von willebrand disease, type 1 9.8 F3 F2
84 typhoid fever 9.8 F2 CRP
85 esophageal varix 9.8 F3 F2
86 post-thrombotic syndrome 9.8 F3 F2
87 factor x deficiency 9.8 F3 F2
88 intracranial thrombosis 9.8 F3 F2
89 thrombophilia due to activated protein c resistance 9.8 F3 F2
90 thrombophilia 9.8 F3 F2
91 primary thrombocytopenia 9.8 F3 F2
92 pleural disease 9.8 F2 CRP
93 factor v deficiency 9.8 F3 F2
94 factor xiii deficiency 9.8 F3 F2
95 purpura fulminans 9.8 F3 F2
96 antithrombin iii deficiency 9.8 F3 F2
97 central retinal vein occlusion 9.8 F3 F2
98 retinal vein occlusion 9.8 F3 F2
99 factor viii deficiency 9.8 F3 F2
100 homocysteinemia 9.8 F2 CRP
101 factor xi deficiency 9.8 F3 F2
102 cortical blindness 9.8 F3 F2
103 protein s deficiency 9.7 F3 F2
104 alcoholic hepatitis 9.7 F2 CRP
105 pulmonary edema 9.7 F2 CRP
106 inherited blood coagulation disease 9.7 F3 F2
107 factor vii deficiency 9.7 F3 F2
108 nutritional deficiency disease 9.7 F2 CRP
109 sickle cell anemia 9.7 F2 CRP
110 thrombophilia due to thrombin defect 9.7 F3 F2
111 blood protein disease 9.7 F3 F2
112 atherosclerosis susceptibility 9.7 F3 CRP
113 nephrosclerosis 9.7 F3 F2
114 von willebrand's disease 9.7 F3 F2
115 heart valve disease 9.7 F2 CRP
116 moyamoya disease 1 9.7 F3 F2
117 dengue hemorrhagic fever 9.7 F3 F2
118 budd-chiari syndrome 9.7 F3 F2
119 placental insufficiency 9.7 F3 F2
120 arteries, anomalies of 9.7 F3 CRP
121 biliary tract disease 9.7 F2 CRP
122 hepatitis a 9.7 F3 F2
123 hemophilia b 9.7 F3 F2
124 peritonitis 9.7 F2 CRP
125 glanzmann thrombasthenia 9.7 F3 F2
126 afibrinogenemia, congenital 9.7 F3 F2
127 bernard-soulier syndrome 9.7 F3 F2
128 viral hepatitis 9.7 F2 CRP
129 arteriosclerosis 9.7 F3 CRP
130 hemolytic-uremic syndrome 9.7 F3 F2
131 portal hypertension 9.6 F3 F2
132 inherited metabolic disorder 9.6 F2 CRP
133 familial hypercholesterolemia 9.6 F2 CRP
134 behcet syndrome 9.5 F2 CRP
135 synovial angioma 9.4 F3 F2 CRP
136 renal pelvis squamous cell carcinoma 9.4 F3 F2 CRP
137 blue toe syndrome 9.4 F3 F2 CRP
138 emphysematous cholecystitis 9.4 F3 F2 CRP
139 cavernous sinus thrombosis 9.4 F3 F2 CRP
140 lemierre's syndrome 9.4 F3 F2 CRP
141 ankylosing spondylitis 1 9.4 F3 F2 CRP
142 marantic endocarditis 9.4 F3 F2 CRP
143 intracranial sinus thrombosis 9.4 F3 F2 CRP
144 epidural abscess 9.4 F3 F2 CRP
145 mediastinitis 9.4 F3 F2 CRP
146 intracranial embolism 9.4 F3 F2 CRP
147 splenic infarction 9.4 F3 F2 CRP
148 active peptic ulcer disease 9.4 F3 F2 CRP
149 analbuminemia 9.4 F3 F2 CRP
150 anuria 9.4 F3 F2 CRP
151 cardiac tamponade 9.4 F3 F2 CRP
152 papilledema 9.4 F3 F2 CRP
153 compartment syndrome 9.4 F3 F2 CRP
154 tricuspid valve insufficiency 9.4 F3 F2 CRP
155 tricuspid valve disease 9.4 F3 F2 CRP
156 peripheral vertigo 9.4 F3 F2 CRP
157 cecal disease 9.4 F3 F2 CRP
158 thrombophlebitis 9.4 F3 F2 CRP
159 mitral valve stenosis 9.4 F3 F2 CRP
160 coronary thrombosis 9.4 F3 F2 CRP
161 aspiration pneumonia 9.4 F3 F2 CRP
162 pneumonia 9.4 F3 F2 CRP
163 autoimmune disease of cardiovascular system 9.4 F3 F2 CRP
164 pericardium disease 9.4 F3 F2 CRP
165 endocardium disease 9.4 F3 F2 CRP
166 pulmonary artery disease 9.4 F3 F2 CRP
167 splenic disease 9.4 F3 F2 CRP
168 hepatic vascular disease 9.4 F3 F2 CRP
169 vascular disease 9.4 F3 F2 CRP
170 pericardial effusion 9.4 F3 F2 CRP
171 vein disease 9.4 F3 F2 CRP
172 exanthem 9.4 F3 F2 CRP
173 mitral valve disease 9.4 F3 F2 CRP
174 purpura 9.4 F3 F2 CRP
175 bilirubin metabolic disorder 9.4 F3 F2 CRP
176 hemorrhagic disease 9.4 F3 F2 CRP
177 heart conduction disease 9.4 F3 F2 CRP
178 blood coagulation disease 9.4 F3 F2 CRP
179 takayasu arteritis 9.4 F3 F2 CRP
180 disseminated intravascular coagulation 9.4 F3 F2 CRP
181 placenta disease 9.4 F3 F2 CRP
182 antiphospholipid syndrome 9.4 F3 F2 CRP
183 thrombocytosis 9.4 F3 F2 CRP
184 blood platelet disease 9.4 F3 F2 CRP
185 pulmonary embolism 9.4 F3 F2 CRP
186 cholangitis 9.4 F3 F2 CRP
187 hellp syndrome 9.4 F3 F2 CRP
188 atrial heart septal defect 9.4 F3 F2 CRP
189 peripheral vascular disease 9.4 F3 F2 CRP
190 patent foramen ovale 9.4 F3 F2 CRP
191 speech and communication disorders 9.4 F3 F2 CRP
192 essential thrombocythemia 9.4 F3 F2 CRP
193 lipoprotein quantitative trait locus 9.4 F3 F2 CRP
194 atrial fibrillation 9.4 F3 F2 CRP
195 respiratory failure 9.4 F3 F2 CRP
196 stroke, ischemic 9.4 F3 F2 CRP
197 pulmonary hypertension 9.4 F3 F2 CRP
198 hypothyroidism 9.4 F3 F2 CRP
199 thrombocytopenia 9.4 F3 F2 CRP
200 pre-eclampsia 9.4 F3 F2 CRP
201 cerebrovascular disease 9.2 F2 CRP
202 myocardial infarction 9.2 F3 F2 CRP
203 inflammatory bowel disease 9.2 F3 F2 CRP
204 malaria 9.2 F3 F2 CRP
205 heart disease 9.2 F3 F2 CRP
206 hypertension, essential 9.2 F3 F2 CRP
207 diabetes mellitus 9.1 F3 F2 CRP
208 systemic lupus erythematosus 8.9 F3 F2 CRP

Graphical network of the top 20 diseases related to Achenbach Syndrome:



Diseases related to Achenbach Syndrome

Symptoms & Phenotypes for Achenbach Syndrome

Drugs & Therapeutics for Achenbach Syndrome

Search Clinical Trials , NIH Clinical Center for Achenbach Syndrome

Genetic Tests for Achenbach Syndrome

Anatomical Context for Achenbach Syndrome

MalaCards organs/tissues related to Achenbach Syndrome:

40
Skin

Publications for Achenbach Syndrome

Articles related to Achenbach Syndrome:

(showing 15, show less)
# Title Authors PMID Year
1
Painful ecchymosis of the finger: a case of Achenbach syndrome. 61
31353447 2020
2
Achenbach Syndrome: A Benign Painful Blue Finger with Tip Sparing. 61
31915672 2019
3
[Spontaneous digital hematoma, Achenbach Sindrome.] 61
31833751 2019
4
Achenbach syndrome (paroxysmal finger hematoma). 61
31159682 2019
5
Achenbach syndrome. 61
31133606 2019
6
Analysis of 24 patients with Achenbach's syndrome. 61
31183341 2019
7
Paroxysmal acral haematoma is a more appropriate name for Achenbach syndrome. 61
30430617 2019
8
Personal observations of Achenbach syndrome. 61
29934997 2018
9
The Acutely Blue Finger: Cause for Concern? 61
29734900 2018
10
[Paroxysmal finger haematoma (Achenbach syndrome)]. 61
26774542 2016
11
A case of spontaneous wrist haematoma in Achenbach syndrome. 61
19675046 2009
12
[Raynaud phenomenon in dermatology. Part 1: Pathophysiology and diagnostic approach]. 61
16902805 2006
13
[Recurrent painful cyanosis of fingers and palm. Recurrent paroxysmal finger hematoma (Achenbach syndrome)]. 61
12405037 2002
14
Achenbach syndrome. 61
7888380 1995
15
[Paroxysmal finger hematoma (Achenbach syndrome)]. 61
2373612 1990

Variations for Achenbach Syndrome

Expression for Achenbach Syndrome

Search GEO for disease gene expression data for Achenbach Syndrome.

Pathways for Achenbach Syndrome

Pathways related to Achenbach Syndrome according to GeneCards Suite gene sharing:

(showing 2, show less)
# Super pathways Score Top Affiliating Genes
1
Show member pathways
11.16 F3 F2
2 10.78 F3 F2

GO Terms for Achenbach Syndrome

Biological processes related to Achenbach Syndrome according to GeneCards Suite gene sharing:

(showing 3, show less)
# Name GO ID Score Top Affiliating Genes
1 blood coagulation GO:0007596 9.16 F3 F2
2 hemostasis GO:0007599 8.96 F3 F2
3 acute-phase response GO:0006953 8.62 F2 CRP

Molecular functions related to Achenbach Syndrome according to GeneCards Suite gene sharing:

(showing 1, show less)
# Name GO ID Score Top Affiliating Genes
1 serine-type endopeptidase activity GO:0004252 8.62 F3 F2

Sources for Achenbach Syndrome

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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