Holoprosencephaly 8

Preferred Label : Holoprosencephaly 8;

Symbol : HPE8;

CISMeF acronym : HPE8;

Type : Phenotype or locus, molecular basis unknown;

Description : For a phenotypic description and a discussion of genetic heterogeneity of holoprosencephaly, see HPE1 (236100).;

Prefixed ID : %609408;

Details

Origin ID

609408;

UMLS CUI

C1836254;

Broader ORDO disease(s)
- Holoprosencephaly [ORDO Disease]
Currated CISMeF NLP mapping
- holoprosencephaly 8 [DO Concept]
- holoprosencephaly 8 [MeSH concept]
- holoprosencephaly 8 [MeSH Supplementary Concept]
DO Cross reference
- holoprosencephaly 8 [DO Concept]
ORDO concept(s)
- Holoprosencephaly [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- holoprosencephaly 8 [MeSH Supplementary Concept]
- holoprosencephaly 8 [MeSH concept]
- holoprosencephaly 8 [DO Concept]

Keyword's position in hierarchy(ies) :

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