Hypospadias 3, autosomal

Preferred Label : Hypospadias 3, autosomal;

Symbol : HYSP3;

CISMeF acronym : HYSP3;

Type : Phenotype or locus, molecular basis unknown;

Description : For a phenotypic description and a discussion of genetic heterogeneity of hypospadias, see 300633.;

Inheritance : Autosomal dominant; Multifactorial;

Prefixed ID : %146450;

Details

Origin ID

146450;

UMLS CUI

C2675154;

Broader ORDO disease(s)
- Familial hypospadias [ORDO Disease]
Currated CISMeF NLP mapping
- hypospadias 3, autosomal [MeSH concept]
- hypospadias 3, autosomal [MeSH Supplementary Concept]
DO Cross reference
- hypospadias [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hypospadias [HPO term]
ORDO concept(s)
- Familial hypospadias [ORDO Disease]
- Non-syndromic posterior hypospadias [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- hypospadias 3, autosomal [MeSH Supplementary Concept]
- hypospadias 3, autosomal [MeSH concept]

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