Congenital microcephaly

Symptom Information:

Symptom ID: HPO:0011451
Synonyms:
Head circumference small for gestational age [HPO:0011451]
Congenital microcephaly [OMIM:Congenital microcephaly]
Microcephaly, congenital [OMIM:Microcephaly, congenital]
Quality:
Cross references:
OMIM: "Congenital microcephaly" [OMIM:Congenital microcephaly]
OMIM: "Microcephaly, congenital" [OMIM:Microcephaly, congenital]
Is a (Direct Parents):
HPO         Microcephaly
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)
                         Congenital microcephaly(HPO:0011451)
       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)
                      Congenital microcephaly(HPO:0011451)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

3-phosphoglycerate dehydrogenase deficiency (Orphanet:79351)
ASPARAGINE SYNTHETASE (OMIM:108370)
Congenital intrauterine infection-like syndrome (Orphanet:1229)
Jawad syndrome (Orphanet:313795)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)