Postnatal microcephaly

Symptom Information:

Symptom ID: HPO:0005484
Synonyms:
Deceleration of head growth [HPO:0005484]
Microcephaly, acquired [HPO:0005484]
Microcephaly, postnatal [HPO:0005484]
Postnatal deceleration of head circumference [HPO:0005484]
Deceleration of head growth [OMIM:Deceleration of head growth]
Microcephaly, acquired [OMIM:Microcephaly, acquired]
Microcephaly, postnatal [OMIM:Microcephaly, postnatal]
Postnatal deceleration of head circumference [OMIM:Postnatal deceleration of head circumference]
Postnatal microcephaly [OMIM:Postnatal microcephaly]
Acquired microcephaly (in severe cases) [OMIM:Acquired microcephaly (in severe cases)]
Microcephaly, acquired (in some patients) [OMIM:Microcephaly, acquired (in some patients)]
Microcephaly, postnatal (-2 to 4.4 SD) [OMIM:Microcephaly, postnatal (-2 to 4.4 SD)]
Quality:
Cross references:
OMIM: "Deceleration of head growth" [OMIM:Deceleration of head growth]
OMIM: "Microcephaly, acquired" [OMIM:Microcephaly, acquired]
OMIM: "Microcephaly, postnatal" [OMIM:Microcephaly, postnatal]
OMIM: "Postnatal deceleration of head circumference" [OMIM:Postnatal deceleration of head circumference]
OMIM: "Postnatal microcephaly" [OMIM:Postnatal microcephaly]
OMIM: "Acquired microcephaly (in severe cases)" [OMIM:Acquired microcephaly (in severe cases)]
OMIM: "Microcephaly, acquired (in some patients)" [OMIM:Microcephaly, acquired (in some patients)]
OMIM: "Microcephaly, postnatal (-2 to 4.4 SD)" [OMIM:Microcephaly, postnatal (-2 to 4.4 SD)]
Is a (Direct Parents):
HPO         Microcephaly
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
       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)
MedDRA:
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)