Search results for "intrauterine and postnatal growth retardation"

The MalaCard for "intrauterine and postnatal growth retardation" has been retired.
Searching MalaCards for entries containing "intrauterine and postnatal growth retardation"

194 hits were found for 'intrauterine and postnatal growth retardation'

# Family MCID Name MIFTS Score
1
END072 Endotheliitis 42 0.597
2
INS024 Insulin-Like Growth Factor I 74 0.449
3
P PNC044 Pancreatitis 60 0.299
4
P HPT021 Hepatitis 70 0.298
5
P LKM002 Leukemia 70 0.293
6
P ADN016 Adenocarcinoma 69 0.278
7
P OBS005 Obesity 93 0.275
8
P THY032 Thyroiditis 54 0.271
9
ACD009 Acid-Labile Subunit, Deficiency of 48 0.260
10
HYP266 Hypoxia 55 0.247
11
CRB009 Cerebritis 38 0.246
12
P LYM118 Lymphoma 70 0.233
13
PLC008 Placenta Disease 36 0.223
14
P MCR010 Microcephaly 58 0.220
15
P CRV039 Cervicitis 44 0.219
16
P INF032 Infertility 61 0.195
17
NTR005 Nutritional Deficiency Disease 39 0.193
18
P HRT032 Heart Disease 76 0.191
19
P ESP024 Esophagitis 62 0.178
20
P ECL001 Eclampsia 54 0.176
21
P EPL164 Epilepsy 66 0.175
22
DWR001 Dwarfism 46 0.169
23
P INT063 Intellectual Disability 53 0.168
24
P SCH015 Schizophrenia 76 0.159
25
CCN007 Cocoon Syndrome 35 0.158
26
HV1006 Hiv-1 82 0.157
27
P HYP086 Hypothyroidism 65 0.147
28
P MYP004 Myopathy 67 0.140
29
BWN001 Bowen-Conradi Syndrome 45 0.139
30
CHL071 Child Syndrome 58 0.137
31
P CRD011 Cardiomyopathy 67 0.134
32
P NRP001 Neuropathy 60 0.134
33
HYD002 Hydronephrosis 47 0.134
34
SPS057 Spasticity 42 0.133
35
SXL003 Sexual Disorder 47 0.132
36
P CTR002 Cataract 57 0.131
37
PLC005 Placental Insufficiency 50 0.131
38
ACR002 Acrocapitofemoral Dysplasia 36 0.131
39
P THL005 Thalassemia 61 0.129
40
BRT030 Birth Defects 43 0.128
41
KDS001 Kid Syndrome 53 0.128
42
P ENC018 Encephalopathy 59 0.127
43
MYL020 Myelomeningocele 50 0.127
44
P PRD006 Prader-Willi Syndrome 63 0.125
45
GST033 Gestational Diabetes 56 0.124
46
DSS008 Disease of Mental Health 55 0.123
47
OLG003 Oligohydramnios 52 0.122
48
ADJ001 Adjustment Disorder 38 0.121
49
ACR041 Acromelic Frontonasal Dysostosis 46 0.120
50
ANX002 Anxiety Disorder 69 0.119
51
GLC003 Glucose Intolerance 55 0.117
52
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 29 0.117
53
ALP008 Alopecia 55 0.116
54
CHR008 Choroiditis 43 0.116
55
DWN001 Down Syndrome 65 0.115
56
P HYP265 Hypotonia 39 0.115
57
LRN003 Learning Disability 51 0.114
58
DDN006 Duodenitis 44 0.113
59
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 37 0.113
60
P CNG015 Congenital Diaphragmatic Hernia 58 0.111
61
HYP066 Hyperglycemia 60 0.110
62
P HYD006 Hydrocephalus 67 0.109
63
BRN071 Brain Injury 52 0.109
64
P SLV001 Silver-Russell Syndrome 54 0.109
65
IMG001 Image Syndrome 55 0.109
66
CHR005 Chorioamnionitis 48 0.107
67
P ENC004 Encephalitis 61 0.106
68
GRW004 Growth Retardation with Deafness and Mental Retardation Due to Igf1 Deficiency 41 0.106
69
CRB037 Cerebral Palsy 54 0.106
70
P THR015 Thrombophilia 59 0.103
71
PCK002 Pick Disease 67 0.101
72
ACH004 Achondroplasia 66 0.101
73
CRY002 Cryptorchidism 62 0.101
74
CSY001 C Syndrome 49 0.100
75
P HYP040 Hypospadias 57 0.099
76
MSC004 Muscle Tissue Disease 36 0.099
77
P CRN037 Craniosynostosis 65 0.098
78
P THR014 Thrombocytopenia 64 0.098
79
SXD001 Sex Differentiation Disease 40 0.097
80
P HYP060 Hyperinsulinism 59 0.096
81
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 36 0.096
82
P MSC033 Muscle Disorders 52 0.095
83
RBR001 Roberts Syndrome 59 0.092
84
P OST005 Osteogenesis Imperfecta 67 0.091
85
PPL022 Papilloma 55 0.091
86
SKL017 Skeletal Dysplasias 45 0.091
87
SPC003 Specific Developmental Disorder 40 0.091
88
P HMN010 Hemangioma 60 0.091
89
SKL014 Skeletal Dysplasia 46 0.091
90
CRB045 Cerebellar Hypoplasia 48 0.089
91
c CNG021 Congenital Toxoplasmosis 46 0.088
92
P PRC031 Preeclampsia/eclampsia 1 57 0.088
93
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.088
94
P MRG008 Meier-Gorlin Syndrome 1 44 0.087
95
P PLY006 Polydactyly 55 0.085
96
LPR018 Leprechaunism 59 0.084
97
BLM001 Bloom Syndrome 62 0.083
98
OMP004 Omphalocele 50 0.082
99
SPC010 Speech and Communication Disorders 46 0.081
100
P FTL001 Fetal Alcohol Syndrome 53 0.080
101
LKM006 Leukomalacia 42 0.080
102
PRP030 Purpura 59 0.080
103
TTR001 Tetralogy of Fallot 71 0.080
104
SMT004 Smith-Lemli-Opitz Syndrome 67 0.079
105
EXF001 Exfoliation Syndrome 57 0.079
106
CHL061 Childhood Leukemia 48 0.079
107
ACN011 Acne 63 0.079
108
WLF002 Wolf-Hirschhorn Syndrome 45 0.078
109
CHL068 Cholestasis 58 0.078
110
BLR001 Biliary Atresia 51 0.076
111
DBW001 Dubowitz Syndrome 46 0.076
112
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 41 0.075
113
c CNG124 Congenital Rubella 40 0.075
114
P HLP001 Holoprosencephaly 62 0.075
115
P PLN008 Peeling Skin Syndrome 47 0.075
116
P DYS007 Dyskeratosis Congenita 63 0.074
117
PRV004 Periventricular Leukomalacia 48 0.073
118
ARC002 Arachnoiditis 38 0.072
119
P CFF001 Coffin-Siris Syndrome 50 0.072
120
PLY012 Polyhydramnios 47 0.072
121
NRL016 Neural Tube Defects 76 0.070
122
CHR103 Charge Syndrome 64 0.070
123
P MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 34 0.070
124
EPD016 Epidermolysis Bullosa 57 0.070
125
MNK001 Menkes Disease 61 0.070
126
ART002 Arts Syndrome 53 0.069
127
P BCK002 Beckwith-Wiedemann Syndrome 56 0.069
128
ANN002 Anencephaly 52 0.068
129
WST001 West Syndrome 61 0.068
130
P CRN139 Cornelia De Lange Syndrome 1 60 0.068
131
P MYT002 Myotonic Dystrophy 47 0.067
132
P VNT002 Ventricular Septal Defect 59 0.067
133
P SCK009 Seckel Syndrome 1 46 0.065
134
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 43 0.065
135
ARC007 Arachnoid Cysts 38 0.065
136
BRN003 Branchiooculofacial Syndrome 40 0.064
137
3MS007 3-M Syndrome 1 42 0.064
138
RBS003 Rabson-Mendenhall Syndrome 55 0.063
139
P HYP055 Hypoplastic Left Heart Syndrome 60 0.063
140
DNT012 Dental Caries 46 0.063
141
PTR006 Peters Anomaly 64 0.063
142
PYL006 Pyloric Stenosis 46 0.062
143
PRT011 Protein C Deficiency 51 0.062
144
ALP091 Alopecia-Contractures-Dwarfism Mental Retardation Syndrome 19 0.062
145
GRW028 Growth Retardation, Developmental Delay, Facial Dysmorphism 24 0.061
146
P LSS002 Lissencephaly 49 0.060
147
P ALG002 Alagille Syndrome 72 0.060
148
CRP010 Corpus Callosum Agenesis 40 0.058
149
FLP001 Filippi Syndrome 26 0.057
150
ELL001 Ellis-Van Creveld Syndrome 57 0.057
151
P DGR001 Digeorge Syndrome 52 0.057
152
VTR016 Vater/vacterl Association 46 0.055
153
CHR219 Chromosome 19q13.11 Deletion Syndrome 24 0.055
154
BND015 Band-Like Calcification with Simplified Gyration and Polymicrogyria 46 0.054
155
P MRD002 Marden-Walker Syndrome 46 0.054
156
MYH012 Myhre Syndrome 35 0.054
157
CYT004 Cytomegalic Inclusion Disease 30 0.053
158
P CRB154 Cerebrocostomandibular Syndrome 34 0.053
159
c 3MT014 3-Methylglutaconic Aciduria, Type V 27 0.052
160
c MRG010 Meier-Gorlin Syndrome 3 20 0.052
161
c MRG011 Meier-Gorlin Syndrome 4 20 0.052
162
c MRG009 Meier-Gorlin Syndrome 2 19 0.052
163
c MRG012 Meier-Gorlin Syndrome 5 19 0.052
164
c CCK005 Cockayne Syndrome, Type a 39 0.052
165
PYR016 Pyridoxine Deficiency 36 0.051
166
3PS001 3p- Syndrome 38 0.051
167
OLV002 Oliver Syndrome 44 0.051
168
GRW033 Growth Retardation, Small and Puffy Hands and Feet, and Eczema 17 0.051
169
c EXD008 Exudative Vitreoretinopathy 1 60 0.050
170
PTS001 Patau Syndrome 49 0.049
171
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 35 0.049
172
PHS022 Phosphoserine Phosphatase Deficiency 29 0.049
173
FTL007 Fetal Hydantoin Syndrome 30 0.048
174
c CTS041 Cutis Laxa, Autosomal Dominant 3 22 0.048
175
NLX003 Neu-Laxova Syndrome 2 19 0.048
176
CHR399 Chromosome 4q21 Deletion Syndrome 22 0.047
177
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 26 0.047
178
NTR029 Natural Killer Cell and Glucocorticoid Deficiency with Dna Repair Defect 20 0.047
179
CHR381 Chromosome 17q23.1-Q23.2 Deletion Syndrome 26 0.047
180
WRS002 Warsaw Breakage Syndrome 32 0.045
181
TRS012 Trisomy 22 26 0.045
182
c MRG014 Meier-Gorlin Syndrome 6 10 0.045
183
CLC057 Cole-Carpenter Syndrome 30 0.045
184
c SCK010 Seckel Syndrome 4 27 0.045
185
PLM041 Pulmonary Valve Stenosis 48 0.044
186
NNT024 Neonatal Stroke 37 0.043
187
ACR012 Aicardi Syndrome 45 0.043
188
c CCK006 Cockayne Syndrome, Type B 37 0.042
189
P RTS001 Ritscher-Schinzel Syndrome 32 0.042
190
CTL005 Catel-Manzke Syndrome 31 0.041
191
c CRB099 Cerebrooculofacioskeletal Syndrome 3 17 0.041
192
CRP028 Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence 19 0.040
193
c FNC025 Fanconi Anemia, Complementation Group J 25 0.040
194
LYS010 Lysyl Hydroxylase 3 Deficiency 21 0.040