Red skin pigment anomaly of new guinea

Preferred Label : Red skin pigment anomaly of new guinea;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal recessive;

Prefixed ID : %266350;

Details

Origin ID

266350;

UMLS CUI

C1849451;

Currated CISMeF NLP mapping
- red skin pigment anomaly of new guinea [MeSH concept]
- red skin pigment anomaly of new guinea [MeSH Supplementary Concept]
HPO term(s)
- Abnormal hair morphology [HPO term]
- Autosomal recessive inheritance [HPO term]
- Nystagmus [HPO term]
- Photophobia [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- red skin pigment anomaly of new guinea [MeSH Supplementary Concept]
- red skin pigment anomaly of new guinea [MeSH concept]

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