Anhidrosis, familial generalized, with abnormal or absent sweat glands

Preferred Label : Anhidrosis, familial generalized, with abnormal or absent sweat glands;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 206600;

Details

Origin ID

206600;

UMLS CUI

C4225670;

Currated CISMeF NLP mapping
- ANHIDROSIS [WHO-ART Included Term]
- Anhidrosis [PASCAL descriptor]
- Anhidrosis [ICD-10 Sub-category]
- Anhidrosis [ICD-10 Sub-category (who)]
- Anhidrosis [HPO term]
- Anhidrosis [MedDRA Preferred Term]
- Anhidrosis [NCIt concept]
- Anhidrosis [ICD-9 code]
- Anhidrosis (disorder) [SNOMED CT concept]
- Anhydrosis [MedDRA LLT]
- anhidrosis [DO Concept]
- anhidrosis [Disease (Nov.)]
- anhidrosis [MeSH concept]
- anhidrosis [SNOMED Notion]
DO Cross reference
- anhidrosis [DO Concept]
HPO term(s)
- Abnormality of the dentition [HPO term]
- Abnormality of the nervous system [HPO term]
- Anhidrosis [HPO term]
- Aplasia of the sweat glands [HPO term]
- Autosomal recessive inheritance [HPO term]
- Dry skin [HPO term]
- Palmoplantar hyperkeratosis [HPO term]
Not associated HPO term(s)
- Abnormal facial shape [HPO term]
- Abnormal hair morphology [HPO term]
- Abnormality of the nail [HPO term]
- Growth abnormality [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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