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"

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

# Family MCID Name MIFTS Score
1
END072 Endotheliitis 42 0.577
2
INS024 Insulin-Like Growth Factor I 75 0.429
3
P HPT021 Hepatitis 69 0.291
4
P PNC044 Pancreatitis 61 0.290
5
P LKM002 Leukemia 71 0.287
6
P ADN016 Adenocarcinoma 69 0.272
7
P THY032 Thyroiditis 54 0.262
8
P OBS005 Obesity 92 0.260
9
ACD009 Acid-Labile Subunit, Deficiency of 45 0.254
10
HYP266 Hypoxia 56 0.242
11
CRB009 Cerebritis 39 0.235
12
P LYM118 Lymphoma 69 0.227
13
PLC008 Placenta Disease 33 0.224
14
P CRV039 Cervicitis 45 0.214
15
P MCR010 Microcephaly 58 0.208
16
P INF032 Infertility 59 0.191
17
NTR005 Nutritional Deficiency Disease 36 0.190
18
P HRT032 Heart Disease 75 0.189
19
P ESP024 Esophagitis 61 0.175
20
c PRC016 Pre-Eclampsia 56 0.172
21
P ECL001 Eclampsia 54 0.171
22
P EPL164 Epilepsy 66 0.162
23
DWR001 Dwarfism 47 0.160
24
CCN007 Cocoon Syndrome 45 0.158
25
P INT063 Intellectual Disability 49 0.156
26
P SCH015 Schizophrenia 77 0.154
27
BWN001 Bowen-Conradi Syndrome 44 0.143
28
P HYP086 Hypothyroidism 64 0.141
29
PRT036 Peritonitis 63 0.138
30
P MYP004 Myopathy 67 0.132
31
P NRP001 Neuropathy 59 0.129
32
P CRD011 Cardiomyopathy 68 0.129
33
HYD002 Hydronephrosis 47 0.128
34
CHL071 Child Syndrome 58 0.128
35
CYT008 Cytomegalovirus Infection 52 0.127
36
SPS057 Spasticity 42 0.127
37
OVR063 Overnutrition 50 0.127
38
PLC005 Placental Insufficiency 50 0.127
39
ACR002 Acrocapitofemoral Dysplasia 33 0.126
40
P THL005 Thalassemia 64 0.124
41
P CTR002 Cataract 58 0.124
42
SXL003 Sexual Disorder 42 0.124
43
KDS001 Kid Syndrome 53 0.123
44
BRT030 Birth Defects 43 0.123
45
GST033 Gestational Diabetes 57 0.122
46
P ENC018 Encephalopathy 59 0.121
47
P MSC005 Muscular Dystrophy 65 0.120
48
P PRD006 Prader-Willi Syndrome 62 0.119
49
OLG003 Oligohydramnios 53 0.119
50
DSS008 Disease of Mental Health 52 0.118
51
LNG099 Lung Disease 64 0.117
52
ADJ001 Adjustment Disorder 38 0.117
53
ACR041 Acromelic Frontonasal Dysostosis 45 0.117
54
ANX002 Anxiety Disorder 67 0.115
55
ACQ007 Acquired Immunodeficiency Syndrome 60 0.115
56
GLC003 Glucose Intolerance 55 0.113
57
CHR008 Choroiditis 44 0.112
58
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.111
59
P HYP265 Hypotonia 38 0.110
60
DWN001 Down Syndrome 66 0.110
61
ALP008 Alopecia 57 0.110
62
ADM013 Adamantinoma of Long Bones 57 0.109
63
BLD054 Blood Protein Disease 37 0.109
64
P CNG015 Congenital Diaphragmatic Hernia 60 0.109
65
DDN006 Duodenitis 42 0.109
66
LRN003 Learning Disability 49 0.109
67
BRN071 Brain Injury 52 0.108
68
GRW004 Growth Retardation with Deafness and Mental Retardation Due to Igf1 Deficiency 39 0.107
69
PRM097 Primary Immunodeficiency Disease 60 0.107
70
HYP066 Hyperglycemia 61 0.106
71
P HYD006 Hydrocephalus 66 0.105
72
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 38 0.104
73
IMG001 Image Syndrome 50 0.103
74
CHR005 Chorioamnionitis 48 0.103
75
P SLV001 Silver-Russell Syndrome 54 0.103
76
PCK002 Pick Disease 68 0.102
77
P SPS003 Spastic Diplegia 52 0.102
78
CRB037 Cerebral Palsy 66 0.102
79
MSC004 Muscle Tissue Disease 34 0.101
80
P ENC004 Encephalitis 63 0.101
81
CSY001 C Syndrome 50 0.099
82
AYM001 Ayme-Gripp Syndrome 41 0.099
83
ACH004 Achondroplasia 66 0.099
84
P THR015 Thrombophilia 59 0.097
85
P NRV007 Nervous System Disease 71 0.095
86
SXD001 Sex Differentiation Disease 38 0.095
87
CRY002 Cryptorchidism 60 0.095
88
P THR014 Thrombocytopenia 64 0.094
89
P HYP040 Hypospadias 57 0.094
90
P CRN037 Craniosynostosis 66 0.093
91
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.092
92
RBR001 Roberts Syndrome 60 0.092
93
P MSC033 Muscle Disorders 52 0.092
94
P HYP060 Hyperinsulinism 58 0.091
95
URT001 Urethritis 41 0.090
96
P HMN010 Hemangioma 59 0.090
97
P TRT010 Teratoma 52 0.089
98
IMM136 Immune System Disease 51 0.088
99
SPC003 Specific Developmental Disorder 38 0.088
100
P OST005 Osteogenesis Imperfecta 69 0.088
101
SKL014 Skeletal Dysplasia 46 0.086
102
PPL022 Papilloma 55 0.086
103
c CNG021 Congenital Toxoplasmosis 48 0.086
104
SKL017 Skeletal Dysplasias 45 0.086
105
P PRC031 Preeclampsia/eclampsia 1 51 0.085
106
CRB045 Cerebellar Hypoplasia 48 0.084
107
P PLY018 Polycythemia 58 0.083
108
BLM001 Bloom Syndrome 63 0.083
109
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.083
110
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 34 0.082
111
INT051 Intussusception 50 0.082
112
OMP004 Omphalocele 50 0.081
113
SPC010 Speech and Communication Disorders 41 0.080
114
P PLY006 Polydactyly 56 0.079
115
WLF002 Wolf-Hirschhorn Syndrome 49 0.079
116
P MRG008 Meier-Gorlin Syndrome 1 45 0.078
117
LPR018 Leprechaunism 58 0.078
118
SMT004 Smith-Lemli-Opitz Syndrome 66 0.078
119
CHL061 Childhood Leukemia 49 0.078
120
CRN036 Craniopharyngioma 59 0.077
121
LKM006 Leukomalacia 43 0.077
122
PRP030 Purpura 58 0.077
123
EXF001 Exfoliation Syndrome 57 0.077
124
DBW001 Dubowitz Syndrome 41 0.077
125
TTR001 Tetralogy of Fallot 71 0.076
126
P FTL001 Fetal Alcohol Syndrome 53 0.075
127
CHL068 Cholestasis 59 0.075
128
P CRN015 Cornelia De Lange Syndrome 62 0.074
129
BLR001 Biliary Atresia 52 0.073
130
P PLN008 Peeling Skin Syndrome 45 0.073
131
P HLP001 Holoprosencephaly 63 0.072
132
c CNG124 Congenital Rubella 44 0.072
133
PRV004 Periventricular Leukomalacia 48 0.071
134
P DYS007 Dyskeratosis Congenita 63 0.070
135
TWN001 Twin-to-Twin Transfusion Syndrome 48 0.070
136
ARC002 Arachnoiditis 41 0.069
137
PLY012 Polyhydramnios 47 0.068
138
P BCK002 Beckwith-Wiedemann Syndrome 56 0.068
139
CNG368 Congenital Adrenal Hyperplasia 62 0.068
140
P CFF001 Coffin-Siris Syndrome 51 0.067
141
ART002 Arts Syndrome 51 0.067
142
MNK001 Menkes Disease 60 0.066
143
NRL016 Neural Tube Defects 76 0.066
144
c MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 44 0.066
145
CHR103 Charge Syndrome 62 0.066
146
WST001 West Syndrome 57 0.065
147
P MYT002 Myotonic Dystrophy 48 0.065
148
P VNT002 Ventricular Septal Defect 60 0.064
149
P SYP003 Syphilis 53 0.064
150
ANN002 Anencephaly 54 0.064
151
c PST041 Posterior Urethral Valves 47 0.063
152
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.063
153
3MS007 3-M Syndrome 1 43 0.063
154
P HYP055 Hypoplastic Left Heart Syndrome 61 0.062
155
ABL002 Ablepharon-Macrostomia Syndrome 57 0.062
156
ARC007 Arachnoid Cysts 39 0.062
157
DNT012 Dental Caries 46 0.062
158
PRT011 Protein C Deficiency 52 0.061
159
P SCK004 Seckel Syndrome 54 0.060
160
BRN003 Branchiooculofacial Syndrome 41 0.060
161
PYL006 Pyloric Stenosis 46 0.060
162
P LSS002 Lissencephaly 49 0.059
163
PTR006 Peters Anomaly 65 0.059
164
RBS003 Rabson-Mendenhall Syndrome 55 0.057
165
P ALG002 Alagille Syndrome 72 0.057
166
GRW028 Growth Retardation, Developmental Delay, Facial Dysmorphism 23 0.056
167
ADR009 Adrenal Cortex Disease 39 0.056
168
BCT004 Bacteriuria 45 0.055
169
P DGR001 Digeorge Syndrome 53 0.054
170
CRP010 Corpus Callosum Agenesis 38 0.054
171
ELL001 Ellis-Van Creveld Syndrome 58 0.054
172
FLP001 Filippi Syndrome 26 0.053
173
VTR016 Vater/vacterl Association 46 0.053
174
GLL032 Galloway-Mowat Syndrome 51 0.052
175
CHR219 Chromosome 19q13.11 Deletion Syndrome 23 0.052
176
CYT004 Cytomegalic Inclusion Disease 31 0.051
177
c 3MT014 3-Methylglutaconic Aciduria, Type V 36 0.051
178
ALP091 Alopecia-Contractures-Dwarfism Mental Retardation Syndrome 19 0.051
179
c EXD008 Exudative Vitreoretinopathy 1 59 0.050
180
P CRB154 Cerebrocostomandibular Syndrome 36 0.049
181
c MRG010 Meier-Gorlin Syndrome 3 21 0.049
182
c MRG011 Meier-Gorlin Syndrome 4 20 0.049
183
c MRG009 Meier-Gorlin Syndrome 2 20 0.049
184
c MRG012 Meier-Gorlin Syndrome 5 19 0.049
185
PYR016 Pyridoxine Deficiency 36 0.049
186
PTS001 Patau Syndrome 49 0.049
187
c CCK005 Cockayne Syndrome, Type a 39 0.049
188
PRN019 Perinatal Necrotizing Enterocolitis 42 0.049
189
TRS012 Trisomy 22 27 0.048
190
c SCK009 Seckel Syndrome 1 40 0.048
191
3PS001 3p- Syndrome 38 0.048
192
FTL007 Fetal Hydantoin Syndrome 32 0.048
193
GRW033 Growth Retardation, Small and Puffy Hands and Feet, and Eczema 17 0.047
194
P RTS001 Ritscher-Schinzel Syndrome 42 0.047
195
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 35 0.046
196
PHS022 Phosphoserine Phosphatase Deficiency 30 0.046
197
NLX003 Neu-Laxova Syndrome 2 22 0.046
198
MYH012 Myhre Syndrome 38 0.046
199
c CTS041 Cutis Laxa, Autosomal Dominant 3 22 0.045
200
CHR381 Chromosome 17q23.1-Q23.2 Deletion Syndrome 27 0.045
201
CHR399 Chromosome 4q21 Deletion Syndrome 22 0.045
202
c DYS152 Dyskeratosis Congenita, Autosomal Recessive 5 26 0.045
203
c CNG033 Congenital Syphilis 39 0.044
204
P MRD002 Marden-Walker Syndrome 46 0.044
205
NTR029 Natural Killer Cell and Glucocorticoid Deficiency with Dna Repair Defect 20 0.044
206
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 26 0.043
207
CLC057 Cole-Carpenter Syndrome 33 0.042
208
c MRG014 Meier-Gorlin Syndrome 6 11 0.042
209
WRS002 Warsaw Breakage Syndrome 30 0.042
210
c CRN139 Cornelia De Lange Syndrome 1 48 0.042
211
c SCK010 Seckel Syndrome 4 28 0.042
212
NNT024 Neonatal Stroke 36 0.041
213
ACR012 Aicardi Syndrome 46 0.041
214
MSC077 Muscle Eye Brain Disease 57 0.041
215
P HYP097 Hyperekplexia 54 0.040
216
c CCK006 Cockayne Syndrome, Type B 37 0.040
217
CTL005 Catel-Manzke Syndrome 31 0.039
218
c CRB099 Cerebrooculofacioskeletal Syndrome 3 18 0.039
219
c FNC025 Fanconi Anemia, Complementation Group J 25 0.038
220
LYS010 Lysyl Hydroxylase 3 Deficiency 21 0.037