Postnatal microcephaly
Symptom Information:
Symptom ID: | HPO:0005484 | ||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal axial skeleton morphology(HPO:0009121) Abnormality of the skull(HPO:0000929) Abnormality of skull size(HPO:0000240) Microcephaly(HPO:0000252) Postnatal microcephaly(HPO:0005484) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the skull(HPO:0000929) Abnormality of skull size(HPO:0000240) Microcephaly(HPO:0000252) Postnatal microcephaly(HPO:0005484) MedDRA: |
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Database Frequency: | 32 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
8q22.1 microdeletion syndrome | (Orphanet:178303) |
Angelman syndrome | (Orphanet:72) |
BARAITSER-WINTER SYNDROME 2 | (OMIM:614583) |
CLN1 disease | (Orphanet:228329) |
Congenital muscular dystrophy with intellectual disability and severe epilepsy | (Orphanet:329178) |
Constitutional megaloblastic anemia with severe neurologic disease | (Orphanet:319651) |
DK1-CDG | (Orphanet:91131) |
DPM1-CDG | (Orphanet:79322) |
Dravet syndrome | (Orphanet:33069) |
Encephalopathy due to GLUT1 deficiency | (Orphanet:71277) |
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome | (Orphanet:319678) |
Intellectual deficit, X-linked, Cantagrel type | (Orphanet:85277) |
Intellectual deficit, X-linked, Schimke type | (Orphanet:85285) |
LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA | (OMIM:608809) |
Lissencephaly due to LIS1 mutation | (Orphanet:95232) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13 | (OMIM:613192) |
MICROCEPHALY WITH SPASTIC QUADRIPLEGIA | (OMIM:251280) |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY | (OMIM:613668) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
Pelizaeus-Merzbacher-like due to HSPD1 mutation | (Orphanet:280288) |
Phosphoserine aminotransferase deficiency | (Orphanet:284417) |
Pontocerebellar hypoplasia type 8 | (Orphanet:324569) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
Porencephaly-microcephaly-bilateral congenital cataract syndrome | (Orphanet:306547) |
Progressive myoclonic epilepsy with dystonia | (Orphanet:352596) |
Recombinant 8 syndrome | (Orphanet:96167) |
Rett syndrome | (Orphanet:778) |
TMEM165-CDG | (Orphanet:314667) |
Tetrasomy 12p | (Orphanet:884) |
WARBURG MICRO SYNDROME 2 | (OMIM:614225) |
WARBURG MICRO SYNDROME 3 | (OMIM:614222) |
WARBURG MICRO SYNDROME 4 | (OMIM:615663) |