Split-hand/foot malformation with long bone deficiency 2

Preferred Label : Split-hand/foot malformation with long bone deficiency 2;

Symbol : SHFLD2;

CISMeF acronym : SHFLD2;

Type : Phenotype or locus, molecular basis unknown;

Description : For a general phenotypic description and discussion of genetic heterogeneity of split-hand/foot malformation with long bone deficiency, see SHFLD1 (119100).;

Prefixed ID : %610685;

Details

Origin ID

610685;

UMLS CUI

C1853156;

Currated CISMeF NLP mapping
- Split-Hand-Foot Malformation With Long Bone Deficiency 2 [MeSH concept]
- Split-Hand-Foot Malformation With Long Bone Deficiency 2 [MeSH Supplementary Concept]
ORDO concept(s)
- Tibial aplasia-ectrodactyly syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Split-Hand-Foot Malformation With Long Bone Deficiency 2 [MeSH Supplementary Concept]
- Split-Hand-Foot Malformation With Long Bone Deficiency 2 [MeSH concept]

Keyword's position in hierarchy(ies) :

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