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"

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

# Family MCID Name MIFTS Score
1
WLF002 Wolf-Hirschhorn Syndrome 50 3.538
2
END072 Endotheliitis 41 0.618
3
INS024 Insulin-Like Growth Factor I 75 0.463
4
P HPT021 Hepatitis 74 0.305
5
P PNC044 Pancreatitis 62 0.303
6
P LKM002 Leukemia 70 0.299
7
P OBS005 Obesity 91 0.283
8
P ADN016 Adenocarcinoma 69 0.283
9
P THY032 Thyroiditis 57 0.275
10
ACD009 Acid-Labile Subunit, Deficiency of 37 0.261
11
CRB009 Cerebritis 36 0.253
12
HYP266 Hypoxia 55 0.251
13
P MCR010 Microcephaly 60 0.240
14
P LYM118 Lymphoma 68 0.236
15
P CRV039 Cervicitis 45 0.224
16
PLC008 Placenta Disease 33 0.220
17
P INT063 Intellectual Disability 46 0.200
18
P INF032 Infertility 61 0.194
19
NTR005 Nutritional Deficiency Disease 51 0.189
20
P ESP024 Esophagitis 62 0.181
21
P ECL001 Eclampsia 55 0.179
22
c PRC016 Pre-Eclampsia 57 0.179
23
DWR001 Dwarfism 42 0.176
24
P EPL164 Epilepsy 60 0.175
25
P HRT032 Heart Disease 64 0.168
26
c CNG401 Congenital Heart Disease 67 0.162
27
P SCH015 Schizophrenia 78 0.161
28
CCN007 Cocoon Syndrome 32 0.157
29
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 32 0.154
30
SPS057 Spasticity 41 0.149
31
P ENC018 Encephalopathy 59 0.148
32
P MYP004 Myopathy 67 0.146
33
P HYP086 Hypothyroidism 63 0.143
34
BWN001 Bowen-Conradi Syndrome 51 0.140
35
CHL071 Child Syndrome 58 0.138
36
P CTR002 Cataract 57 0.138
37
P NRP001 Neuropathy 57 0.138
38
P CRD011 Cardiomyopathy 66 0.137
39
HYD002 Hydronephrosis 48 0.136
40
ACR002 Acrocapitofemoral Dysplasia 35 0.132
41
PLC005 Placental Insufficiency 50 0.130
42
MYL020 Myelomeningocele 50 0.130
43
P THL005 Thalassemia 61 0.129
44
KDS001 Kid Syndrome 53 0.129
45
DSS008 Disease of Mental Health 48 0.128
46
P PRD006 Prader-Willi Syndrome 64 0.128
47
BRT030 Birth Defects 44 0.127
48
OLG003 Oligohydramnios 52 0.124
49
P HYP265 Hypotonia 39 0.124
50
ALP008 Alopecia 56 0.123
51
ADJ001 Adjustment Disorder 38 0.120
52
CHR008 Choroiditis 43 0.120
53
GLC003 Glucose Intolerance 56 0.120
54
GST033 Gestational Diabetes 54 0.118
55
DWN001 Down Syndrome 65 0.116
56
ANX002 Anxiety Disorder 67 0.115
57
ACR041 Acromelic Frontonasal Dysostosis 45 0.115
58
DDN006 Duodenitis 44 0.114
59
SXL003 Sexual Disorder 45 0.114
60
LRN003 Learning Disability 49 0.113
61
P HYD006 Hydrocephalus 68 0.113
62
HYP066 Hyperglycemia 61 0.113
63
P SLV001 Silver-Russell Syndrome 54 0.112
64
P CNG015 Congenital Diaphragmatic Hernia 58 0.112
65
CHR005 Chorioamnionitis 47 0.111
66
IMG001 Image Syndrome 54 0.111
67
BRN071 Brain Injury 51 0.110
68
BLD054 Blood Protein Disease 38 0.109
69
CRB037 Cerebral Palsy 54 0.108
70
P ENC004 Encephalitis 60 0.107
71
GRW004 Growth Retardation with Deafness and Mental Retardation Due to Igf1 Deficiency 40 0.107
72
P THR015 Thrombophilia 59 0.107
73
P CRN037 Craniosynostosis 66 0.105
74
P HYP040 Hypospadias 58 0.105
75
CRY002 Cryptorchidism 61 0.104
76
ACH004 Achondroplasia 64 0.103
77
CSY001 C Syndrome 49 0.103
78
MSC004 Muscle Tissue Disease 35 0.102
79
SXD001 Sex Differentiation Disease 39 0.099
80
P HYP060 Hyperinsulinism 58 0.099
81
P MSC033 Muscle Disorders 52 0.097
82
SKL017 Skeletal Dysplasias 41 0.096
83
SKL014 Skeletal Dysplasia 44 0.096
84
CRB045 Cerebellar Hypoplasia 47 0.095
85
P OST005 Osteogenesis Imperfecta 68 0.095
86
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 35 0.094
87
RBR001 Roberts Syndrome 61 0.092
88
PPL022 Papilloma 54 0.092
89
SPC003 Specific Developmental Disorder 39 0.091
90
P HMN010 Hemangioma 62 0.091
91
P PLY006 Polydactyly 56 0.090
92
P PRC031 Preeclampsia/eclampsia 1 53 0.089
93
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 60 0.089
94
LPR018 Leprechaunism 59 0.089
95
c CNG021 Congenital Toxoplasmosis 46 0.088
96
P MRG008 Meier-Gorlin Syndrome 1 46 0.087
97
P PLY018 Polycythemia 58 0.086
98
BLM001 Bloom Syndrome 63 0.084
99
PRP030 Purpura 60 0.083
100
OMP004 Omphalocele 51 0.082
101
P FTL001 Fetal Alcohol Syndrome 53 0.082
102
ACN011 Acne 63 0.082
103
TTR001 Tetralogy of Fallot 69 0.080
104
SPC010 Speech and Communication Disorders 42 0.080
105
LKM006 Leukomalacia 41 0.080
106
P HLP001 Holoprosencephaly 62 0.080
107
SMT004 Smith-Lemli-Opitz Syndrome 66 0.079
108
CHL061 Childhood Leukemia 47 0.079
109
EXF001 Exfoliation Syndrome 56 0.078
110
CHL068 Cholestasis 57 0.078
111
EPD016 Epidermolysis Bullosa 59 0.078
112
DBW001 Dubowitz Syndrome 48 0.078
113
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 42 0.077
114
NRL016 Neural Tube Defects 76 0.077
115
BLR001 Biliary Atresia 52 0.076
116
P CFF001 Coffin-Siris Syndrome 55 0.076
117
c CNG124 Congenital Rubella 40 0.076
118
P HYP076 Hyperthyroidism 59 0.075
119
ARC002 Arachnoiditis 38 0.075
120
P PLN008 Peeling Skin Syndrome 45 0.074
121
PLY012 Polyhydramnios 45 0.074
122
PRV004 Periventricular Leukomalacia 51 0.073
123
P DYS007 Dyskeratosis Congenita 64 0.073
124
P CRN015 Cornelia De Lange Syndrome 65 0.072
125
ANN002 Anencephaly 50 0.071
126
CHR103 Charge Syndrome 64 0.070
127
P BCK002 Beckwith-Wiedemann Syndrome 56 0.070
128
MNK001 Menkes Disease 61 0.070
129
P GNG009 Gangliosidosis 58 0.069
130
ARC007 Arachnoid Cysts 39 0.068
131
RBS003 Rabson-Mendenhall Syndrome 55 0.068
132
P VNT002 Ventricular Septal Defect 59 0.067
133
P MYT002 Myotonic Dystrophy 46 0.067
134
c MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 35 0.066
135
P HYP055 Hypoplastic Left Heart Syndrome 60 0.066
136
ART002 Arts Syndrome 53 0.065
137
WST001 West Syndrome 61 0.065
138
BRN003 Branchiooculofacial Syndrome 51 0.065
139
PRT011 Protein C Deficiency 52 0.065
140
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 42 0.064
141
3MS007 3-M Syndrome 1 42 0.064
142
P SCK004 Seckel Syndrome 53 0.064
143
P LSS002 Lissencephaly 48 0.064
144
PTR006 Peters Anomaly 64 0.064
145
PYL006 Pyloric Stenosis 46 0.064
146
DNT012 Dental Caries 45 0.063
147
GRW028 Growth Retardation, Developmental Delay, Facial Dysmorphism 23 0.062
148
ALP091 Alopecia-Contractures-Dwarfism Mental Retardation Syndrome 20 0.062
149
CRP010 Corpus Callosum Agenesis 38 0.060
150
P ALG002 Alagille Syndrome 70 0.060
151
BND015 Band-Like Calcification with Simplified Gyration and Polymicrogyria 45 0.059
152
FLP001 Filippi Syndrome 27 0.058
153
ELL001 Ellis-Van Creveld Syndrome 56 0.058
154
P DGR001 Digeorge Syndrome 52 0.057
155
P MRD002 Marden-Walker Syndrome 39 0.056
156
VTR016 Vater/vacterl Association 37 0.055
157
MYH012 Myhre Syndrome 37 0.054
158
CHR219 Chromosome 19q13.11 Deletion Syndrome 23 0.054
159
CYT004 Cytomegalic Inclusion Disease 29 0.053
160
P CRB154 Cerebrocostomandibular Syndrome 33 0.053
161
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 34 0.053
162
c MRG011 Meier-Gorlin Syndrome 4 21 0.053
163
c MRG009 Meier-Gorlin Syndrome 2 20 0.053
164
c MRG010 Meier-Gorlin Syndrome 3 21 0.053
165
c MRG012 Meier-Gorlin Syndrome 5 20 0.053
166
c MSC106 Mosaic Variegated Aneuploidy Syndrome 2 23 0.052
167
OLV002 Oliver Syndrome 44 0.052
168
c 3MT014 3-Methylglutaconic Aciduria, Type V 21 0.052
169
c CCK005 Cockayne Syndrome, Type a 39 0.052
170
PYR016 Pyridoxine Deficiency 28 0.051
171
TRS012 Trisomy 22 26 0.051
172
GRW033 Growth Retardation, Small and Puffy Hands and Feet, and Eczema 18 0.051
173
3PS001 3p- Syndrome 38 0.051
174
FTL007 Fetal Hydantoin Syndrome 28 0.051
175
PTS001 Patau Syndrome 49 0.050
176
PHS022 Phosphoserine Phosphatase Deficiency 28 0.049
177
c CTS041 Cutis Laxa, Autosomal Dominant 3 22 0.049
178
NLX003 Neu-Laxova Syndrome 2 19 0.049
179
PLM041 Pulmonary Valve Stenosis 48 0.048
180
CHR381 Chromosome 17q23.1-Q23.2 Deletion Syndrome 29 0.048
181
CHR399 Chromosome 4q21 Deletion Syndrome 22 0.047
182
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 27 0.047
183
NTR029 Natural Killer Cell and Glucocorticoid Deficiency with Dna Repair Defect 23 0.047
184
CNG233 Congenital Herpes Virus Infection 17 0.047
185
CLC057 Cole-Carpenter Syndrome 33 0.045
186
c CRN139 Cornelia De Lange Syndrome 1 37 0.045
187
WRS002 Warsaw Breakage Syndrome 33 0.045
188
c MRG014 Meier-Gorlin Syndrome 6 11 0.045
189
c SCK010 Seckel Syndrome 4 28 0.045
190
ACR012 Aicardi Syndrome 45 0.045
191
c CCK006 Cockayne Syndrome, Type B 37 0.043
192
P RTS001 Ritscher-Schinzel Syndrome 35 0.042
193
CTL005 Catel-Manzke Syndrome 32 0.041
194
c CRB099 Cerebrooculofacioskeletal Syndrome 3 18 0.041
195
CRP028 Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence 20 0.040
196
c FNC025 Fanconi Anemia, Complementation Group J 27 0.040
197
LYS010 Lysyl Hydroxylase 3 Deficiency 22 0.040