Acrocephalopolysyndactyly type IV (disorder)
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http://snomed.info/id/733425005
Goodman syndrome is an extremely rare genetic disorder with characteristics of marked malformations of the head and face (essentially acrocephaly), abnormalities of the hands and feet (polydactyly, syndactyly, clinodactyly, camptodactyly, ulnar deviation), and congenital heart disease. There have been no further descriptions in the literature since 1979. Goodman syndrome could be a variant of Carpenter syndrome.
Term info
Label
Acrocephalopolysyndactyly type IV (disorder)
Synonyms
- Acrocephalopolysyndactyly type 4
- Acrocephalopolysyndactyly type IV
- Goodman syndrome
Term relations
Subclass of:
- Acrocephalopolysyndactyly (disorder)
- Hereditary disorder of musculoskeletal system (disorder)
- Autosomal recessive hereditary disorder (disorder)
- Developmental hereditary disorder (disorder)
- Autosomal recessive hereditary disorder (disorder) and Acrocephalopolysyndactyly (disorder) and Role group (attribute) some (
Associated morphology (attribute) some Congenital abnormal fusion (morphologic abnormality) and
Occurrence (attribute) some Congenital (qualifier value) and
Finding site (attribute) some Digit structure (body structure) and
Pathological process (attribute) some Pathological developmental process (qualifier value)) and Role group (attribute) some (
Associated morphology (attribute) some Congenital premature fusion (morphologic abnormality) and
Occurrence (attribute) some Congenital (qualifier value) and
Finding site (attribute) some Joint structure of suture of skull (body structure) and
Pathological process (attribute) some Pathological developmental process (qualifier value)) and Role group (attribute) some (
Associated morphology (attribute) some Supernumerary structure (morphologic abnormality) and
Occurrence (attribute) some Congenital (qualifier value) and
Finding site (attribute) some Digit structure (body structure) and
Pathological process (attribute) some Pathological developmental process (qualifier value))