Progressive microcephaly
Symptom Information:
Symptom ID: | HPO:0000253 | |||||||||||
Synonyms: |
|
|||||||||||
Quality: | ||||||||||||
Cross references: |
|
|||||||||||
Is a (Direct Parents): |
|
|||||||||||
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) Progressive microcephaly(HPO:0000253) 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) Progressive microcephaly(HPO:0000253) MedDRA: |
|||||||||||
Database Frequency: | 37 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
AICARDI-GOUTIERES SYNDROME 1 | (OMIM:225750) |
AICARDI-GOUTIERES SYNDROME 3 | (OMIM:610329) |
AICARDI-GOUTIERES SYNDROME 4 | (OMIM:610333) |
ASPARAGINE SYNTHETASE DEFICIENCY | (OMIM:615574) |
Amish lethal microcephaly | (Orphanet:99742) |
Atypical Rett syndrome | (Orphanet:3095) |
CEDNIK syndrome | (Orphanet:66631) |
CLN1 disease | (Orphanet:228329) |
COG1-CDG | (Orphanet:263508) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2 | (OMIM:300672) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 | (OMIM:613477) |
Early myoclonic encephalopathy | (Orphanet:1935) |
GTP cyclohydrolase I deficiency | (Orphanet:2102) |
Gaucher disease type 2 | (Orphanet:77260) |
Infantile cerebellar-retinal degeneration | (Orphanet:313850) |
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY | (OMIM:613668) |
MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLARATROPHY | (OMIM:615760) |
MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY | (OMIM:614741) |
Mandibulofacial dysostosis-microcephaly syndrome | (Orphanet:79113) |
Microcephaly - seizures - developmental delay | (Orphanet:228418) |
Microcephaly-capillary malformation syndrome | (Orphanet:294016) |
PEHO syndrome | (Orphanet:2836) |
PEHO-like syndrome | (Orphanet:99807) |
PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE | (OMIM:608097) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 1B | (OMIM:614678) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 2A | (OMIM:277470) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 2D | (OMIM:613811) |
Pontocerebellar hypoplasia type 2 | (Orphanet:2524) |
Pontocerebellar hypoplasia type 3 | (Orphanet:97249) |
Pontocerebellar hypoplasia type 6 | (Orphanet:166073) |
Pontocerebellar hypoplasia type 7 | (Orphanet:284339) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
Pyridoxal phosphate-responsive seizures | (Orphanet:79096) |
RETT SYNDROME, CONGENITAL VARIANT | (OMIM:613454) |
Severe neonatal-onset encephalopathy with microcephaly | (Orphanet:209370) |
Wrinkly skin syndrome | (Orphanet:2834) |
X-linked intellectual deficit, Najm type | (Orphanet:163937) |