Leukodystrophy, hypomyelinating, 26, with chondrodysplasia

Preferred Label : Leukodystrophy, hypomyelinating, 26, with chondrodysplasia;

Symbol : HLD26;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Chondrodysplasia with hypomyelinating leukodystrophy;

Prefixed ID : #620269;

Details

Origin ID

620269;

UMLS CUI

C5830312;

Genes related to phenotype
- Solute carrier family 35 (3-prime-phosphoadenosine 5-prime-phosphosulfate transporter), member b2 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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