Search results for intrauterine and postnatal growth retardation

260 hits were found for intrauterine and postnatal growth retardation

# Family MCID Name MIFTS Score
1
END072 Endotheliitis 46 0.620
2
INS024 Insulin-Like Growth Factor I 83 0.477
3
c BLD140 Blood Group, I System 37 0.430
4
AGN016 Aging 65 0.367
5
P HPT021 Hepatitis 75 0.309
6
P PNC044 Pancreatitis 64 0.308
7
P LKM002 Leukemia 75 0.306
8
P ADN016 Adenocarcinoma 71 0.296
9
P THY032 Thyroiditis 56 0.276
10
HYP266 Hypoxia 61 0.255
11
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.255
12
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.254
13
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.254
14
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.254
15
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.254
16
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.254
17
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.254
18
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.254
19
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.254
20
CRB009 Cerebritis 41 0.245
21
P LYM118 Lymphoma 71 0.243
22
P DBT009 Diabetes Mellitus 72 0.233
23
P CRV039 Cervicitis 49 0.227
24
PLC008 Placenta Disease 48 0.226
25
P MCR010 Microcephaly 57 0.221
26
P HRT032 Heart Disease 80 0.210
27
P INF032 Infertility 59 0.208
28
ISC004 Ischemia 66 0.190
29
P ESP024 Esophagitis 64 0.185
30
c PRC016 Pre-Eclampsia 65 0.183
31
P ECL001 Eclampsia 57 0.180
32
DWR001 Dwarfism 48 0.177
33
P EPL164 Epilepsy 70 0.173
34
ANX010 Anxiety 72 0.164
35
P HYP086 Hypothyroidism 62 0.160
36
P SCH015 Schizophrenia 71 0.159
37
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.157
38
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.157
39
ANR040 Aneurysm 61 0.156
40
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.155
41
P ENC018 Encephalopathy 58 0.153
42
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.149
43
PRT036 Peritonitis 67 0.143
44
P NRP001 Neuropathy 63 0.143
45
P TRN020 Turner Syndrome 69 0.143
46
PLC005 Placental Insufficiency 59 0.138
47
P CTR002 Cataract 60 0.136
48
VSC007 Vascular Disease 71 0.132
49
SPS057 Spasticity 41 0.131
50
P PRD006 Prader-Willi Syndrome 66 0.129
51
P THL005 Thalassemia 65 0.129
52
CYT008 Cytomegalovirus Infection 57 0.129
53
HYD002 Hydronephrosis 49 0.128
54
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.126
55
P SLV001 Silver-Russell Syndrome 57 0.126
56
OLG003 Oligohydramnios 41 0.125
57
P HYP265 Hypotonia 40 0.124
58
P RNG031 Ring Chromosome Y Syndrome 29 0.124
59
P ANR048 Aniridia 1 68 0.123
60
GST033 Gestational Diabetes 62 0.122
61
P NRV007 Nervous System Disease 75 0.122
62
GLC003 Glucose Intolerance 58 0.120
63
BRN071 Brain Injury 54 0.118
64
P ALP008 Alopecia 56 0.117
65
HYP066 Hyperglycemia 64 0.116
66
VRL011 Viral Infectious Disease 64 0.115
67
P HYD006 Hydrocephalus 68 0.115
68
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 46 0.115
69
DWN001 Down Syndrome 70 0.114
70
CHR008 Choroiditis 47 0.114
71
NRL016 Neural Tube Defects 79 0.113
72
c DPH024 Diaphragmatic Hernia, Congenital 63 0.112
73
PSY004 Psychotic Disorder 72 0.111
74
DDN006 Duodenitis 46 0.111
75
P ENC004 Encephalitis 66 0.110
76
HYP080 Hypogonadism 54 0.108
77
CRB037 Cerebral Palsy 70 0.107
78
c EXD008 Exudative Vitreoretinopathy 1 65 0.107
79
P THR014 Thrombocytopenia 65 0.107
80
P CRN037 Craniosynostosis 68 0.104
81
P MYP006 Myopia 56 0.104
82
P PLM037 Pulmonary Hypertension 79 0.103
83
ACH004 Achondroplasia 67 0.103
84
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 42 0.102
85
HYP060 Hyperinsulinism 56 0.099
86
URT001 Urethritis 44 0.098
87
P HYP040 Hypospadias 60 0.097
88
P PRC031 Preeclampsia/eclampsia 1 41 0.095
89
c CNG021 Congenital Toxoplasmosis 57 0.095
90
P MRG008 Meier-Gorlin Syndrome 1 42 0.093
91
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.093
92
P PRC019 Precocious Puberty 52 0.093
93
P HMN010 Hemangioma 61 0.092
94
CRB045 Cerebellar Hypoplasia 48 0.089
95
PPL022 Papilloma 58 0.089
96
P THR117 Three M Syndrome 1 52 0.088
97
BRT054 Brittle Bone Disorder 67 0.088
98
SKL017 Skeletal Dysplasias 48 0.088
99
BLM001 Bloom Syndrome 62 0.087
100
ACR099 Acrofacial Dysostosis, Catania Type 31 0.086
101
DBW001 Dubowitz Syndrome 44 0.086
102
WLF002 Wolf-Hirschhorn Syndrome 54 0.086
103
P PLY018 Polycythemia 60 0.085
104
c ALP101 Alpha-Thalassemia 60 0.085
105
HMT018 Hematopoietic Stem Cell Transplantation 58 0.085
106
RBR001 Roberts Syndrome 55 0.084
107
SDD001 Sudden Infant Death Syndrome 61 0.083
108
CRN036 Craniopharyngioma 63 0.082
109
P TTR001 Tetralogy of Fallot 70 0.082
110
P PLY006 Polydactyly 57 0.082
111
P OMP004 Omphalocele 51 0.081
112
LKM006 Leukomalacia 46 0.080
113
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.080
114
c MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 47 0.080
115
PRP030 Purpura 61 0.079
116
c CNG124 Congenital Rubella 47 0.078
117
CHL068 Cholestasis 60 0.078
118
P RBL001 Rubella 61 0.078
119
HYP730 Hypogonadotropic Hypogonadism 56 0.078
120
CHR103 Charge Syndrome 59 0.077
121
P CRN015 Cornelia De Lange Syndrome 65 0.077
122
DNH001 Donohue Syndrome 60 0.077
123
SMT004 Smith-Lemli-Opitz Syndrome 70 0.077
124
P FTL001 Fetal Alcohol Syndrome 59 0.076
125
BLR001 Biliary Atresia 56 0.076
126
P HLP001 Holoprosencephaly 67 0.076
127
MNK001 Menkes Disease 64 0.074
128
PRV004 Periventricular Leukomalacia 53 0.074
129
P DYS007 Dyskeratosis Congenita 68 0.074
130
PLY012 Polyhydramnios 47 0.073
131
BRN003 Branchiooculofacial Syndrome 46 0.072
132
P HYP076 Hyperthyroidism 56 0.072
133
INT102 Intrauterine Growth Retardation with Increased Mitomycin C Sensitivity 14 0.072
134
ARC002 Arachnoiditis 45 0.071
135
HYP064 Hypogonadotropism 38 0.071
136
P CFF008 Coffin-Siris Syndrome 1 59 0.070
137
PRG123 Progeroid Syndrome, Neonatal 30 0.070
138
PTR032 Peters-Plus Syndrome 60 0.070
139
CHL061 Childhood Leukemia 50 0.070
140
FLP001 Filippi Syndrome 32 0.070
141
LPD012 Lipoid Congenital Adrenal Hyperplasia 66 0.069
142
HSH003 Hashimoto Thyroiditis 67 0.069
143
P BCK002 Beckwith-Wiedemann Syndrome 58 0.069
144
P THN009 Thanatophoric Dysplasia, Type I 66 0.068
145
PRT082 Preterm Premature Rupture of the Membranes 51 0.068
146
GRW039 Growth Retardation, Developmental Delay, and Facial Dysmorphism 24 0.067
147
P MYT002 Myotonic Dystrophy 50 0.067
148
ART137 Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect 34 0.067
149
P VNT002 Ventricular Septal Defect 59 0.066
150
CHR379 Chromosome 15q26-Qter Deletion Syndrome 25 0.066
151
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 52 0.066
152
DNT012 Dental Caries 50 0.066
153
P MYC008 Myocarditis 58 0.066
154
BWN001 Bowen-Conradi Syndrome 44 0.066
155
c CCK008 Cockayne Syndrome a 48 0.065
156
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.065
157
NRL018 Neural Tube Defects, Folate-Sensitive 44 0.065
158
RNL039 Renal Dysplasia-Limb Defects Syndrome 27 0.065
159
ANN002 Anencephaly 57 0.065
160
HYD001 Hydranencephaly 36 0.064
161
GRW035 Growth Retardation, Intellectual Developmental Disorder, Hypotonia, and Hepatopathy 18 0.064
162
P MRD002 Marden-Walker Syndrome 47 0.064
163
ARC007 Arachnoid Cysts 39 0.063
164
VTR016 Vater/vacterl Association 37 0.063
165
c KNN009 Kenny-Caffey Syndrome, Type 1 30 0.063
166
CRP032 Corpus Callosum, Agenesis of 40 0.063
167
P SCK004 Seckel Syndrome 55 0.063
168
MYH012 Myhre Syndrome 41 0.062
169
c RTS003 Ritscher-Schinzel Syndrome 1 36 0.062
170
c 3MT014 3-Methylglutaconic Aciduria, Type V 40 0.062
171
OHD004 Ohdo Syndrome 41 0.062
172
P LSS002 Lissencephaly 49 0.062
173
c CCK007 Cockayne Syndrome B 52 0.062
174
P CCK001 Cockayne Syndrome 64 0.062
175
P ALG028 Alagille Syndrome 1 68 0.062
176
c MYT021 Myotonic Dystrophy 1 68 0.061
177
c KNN007 Kenny-Caffey Syndrome, Type 2 30 0.061
178
c SCK009 Seckel Syndrome 1 30 0.061
179
PYL006 Pyloric Stenosis 47 0.061
180
IMM177 Immunodeficiency 54 22 0.061
181
c CTS041 Cutis Laxa, Autosomal Dominant 3 25 0.060
182
DBT083 Diabetes Mellitus, Permanent Neonatal 62 0.060
183
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 37 0.060
184
c MNT295 Mental Retardation, X-Linked, Syndromic 33 25 0.060
185
PYL017 Pyle Disease 49 0.059
186
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 53 0.059
187
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 25 0.059
188
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 37 0.058
189
P CRB154 Cerebrocostomandibular Syndrome 35 0.058
190
c MTR063 Maternal Uniparental Disomy of Chromosome 2 18 0.058
191
CHR616 Chromosome 19q13.11 Deletion Syndrome, Distal 23 0.058
192
c MRG012 Meier-Gorlin Syndrome 5 20 0.057
193
c HYD060 Hydrocephalus, Nonsyndromic, Autosomal Recessive 1 38 0.057
194
c MRG011 Meier-Gorlin Syndrome 4 20 0.057
195
ALP091 Alopecia-Contractures-Dwarfism Mental Retardation Syndrome 24 0.057
196
DBR002 De Barsy Syndrome 38 0.057
197
ELL001 Ellis-Van Creveld Syndrome 61 0.057
198
c MRG009 Meier-Gorlin Syndrome 2 20 0.056
199
WRN004 Wrinkly Skin Syndrome 35 0.056
200
CHR667 Chromosome 3pter-P25 Deletion Syndrome 37 0.056
201
c MRG010 Meier-Gorlin Syndrome 3 23 0.056
202
GRW033 Growth Retardation, Small and Puffy Hands and Feet, and Eczema 20 0.056
203
c GLL038 Galloway-Mowat Syndrome 1 37 0.056
204
CMB047 Combined Oxidative Phosphorylation Deficiency 18 21 0.055
205
c HYD043 Hydrocephalus, Nonsyndromic, Autosomal Recessive 2 36 0.055
206
CHR266 Chromosome 8p23.1 Deletion 27 0.055
207
c TRS012 Trisomy 22 26 0.055
208
DGR001 Digeorge Syndrome 55 0.055
209
c MNT298 Mental Retardation, X-Linked, Syndromic, 35 23 0.055
210
YNS002 Yunis-Varon Syndrome 48 0.054
211
WTT002 Witteveen-Kolk Syndrome 29 0.054
212
CHR399 Chromosome 4q21 Deletion Syndrome 26 0.054
213
CNZ011 Coenzyme Q10 Deficiency, Primary, 8 19 0.054
214
CHR381 Chromosome 17q23.1-Q23.2 Deletion Syndrome 25 0.053
215
IST007 Isotretinoin Embryopathy-Like Syndrome 25 0.053
216
BNF003 Bone Fragility with Contractures, Arterial Rupture, and Deafness 23 0.053
217
WRS002 Warsaw Breakage Syndrome 44 0.053
218
LNZ003 Lenz-Majewski Hyperostotic Dwarfism 35 0.052
219
NLX003 Neu-Laxova Syndrome 2 20 0.052
220
MSC089 Mosaic Monosomy X 22 0.052
221
c TRN055 Turner Syndrome Due to Structural X Chromosome Anomalies 21 0.052
222
CYT004 Cytomegalic Inclusion Disease 35 0.052
223
P PTR018 Paternal Uniparental Disomy of Chromosome 6 23 0.052
224
IMM190 Immunodeficiency 55 14 0.052
225
P LSS036 Lissencephaly, X-Linked, 1 45 0.052
226
ATS238 Autosomal Recessive Cutis Laxa Type 2, Classic Type 32 0.051
227
RFM001 Roifman Syndrome 31 0.051
228
ACR012 Aicardi Syndrome 49 0.051
229
c MRG016 Meier-Gorlin Syndrome 8 15 0.050
230
CNZ009 Coenzyme Q10 Deficiency, Primary, 5 19 0.049
231
c SCK010 Seckel Syndrome 4 26 0.049
232
FTL007 Fetal Hydantoin Syndrome 31 0.049
233
c OTP007 Otopalatodigital Syndrome, Type Ii 38 0.049
234
PHS022 Phosphoserine Phosphatase Deficiency 30 0.049
235
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 22 0.048
236
CTL005 Catel-Manzke Syndrome 35 0.048
237
c CRN139 Cornelia De Lange Syndrome 1 46 0.048
238
DSM002 Desmosterolosis 35 0.047
239
ALK023 Al Kaissi Syndrome 17 0.047
240
c WRB002 Warburg Micro Syndrome 1 42 0.046
241
c CRB099 Cerebrooculofacioskeletal Syndrome 3 20 0.046
242
PTS001 Patau Syndrome 50 0.046
243
c CTS023 Cutis Laxa, Autosomal Recessive, Type Iib 30 0.046
244
CLC057 Cole-Carpenter Syndrome 37 0.045
245
c MRG014 Meier-Gorlin Syndrome 6 21 0.045
246
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 41 0.045
247
STV003 Stuve-Wiedemann Syndrome 38 0.045
248
c MRG015 Meier-Gorlin Syndrome 7 22 0.044
249
BRC091 Brachymorphism-Onychodysplasia-Dysphalangism Syndrome 28 0.044
250
NRD024 Neurodevelopmental Disorder with or Without Anomalies of the Brain, Eye, or Heart 22 0.044
251
c CRN134 Cornelia De Lange Syndrome 2 27 0.043
252
ALP067 Alopecia-Contractures-Dwarfism-Intellectual Disability Syndrome 19 0.043
253
c HYP718 Hyperuricemic Nephropathy, Familial Juvenile, 4 20 0.042
254
c RNG008 Ring Chromosome 13 37 0.042
255
MCR286 Microcephaly-Intellectual Disability-Phalangeal and Neurological Anomalies Syndrome 20 0.042
256
HMF010 Hemifacial Microsomia with Radial Defects 31 0.041
257
CRT027 Cartwright Nelson Fryns Syndrome 6 0.039
258
MTR016 Maternal Hyperphenylalaninemia 18 0.039
259
c FNC025 Fanconi Anemia, Complementation Group J 21 0.038
260
MCR333 Microcephaly, Seizures, Spasticity, and Brain Calcifications 16 0.034
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