Ichthyosis and male hypogonadism

Preferred Label : Ichthyosis and male hypogonadism;

Type : Other, mainly phenotypes with suspected mendelian basis;

Included titles and symbols : Rud syndrome; Ruds;

Inheritance : X-linked (?contiguous gene syndrome);

Prefixed ID : 308200;

Details

Origin ID

308200;

UMLS CUI

C1839989;

Automatic exact mappings (from CISMeF team)
- Ichthyosis and male hypogonadism [MeSH concept]
- Ichthyosis-male hypogonadism syndrome [ORDO Disease]
- Rud Syndrome [MeSH concept]
- Rud's syndrome (disorder) [SNOMED CT concept]
- Xp22.3 microdeletion syndrome [ORDO Disease]
- ichthyosis and male hypogonadism [MeSH Supplementary Concept]
- rud syndrome [MeSH Supplementary Concept]
- rud's syndrome [SNOMED Notion]
HPO term(s)
- Abnormality of metabolism/homeostasis [HPO term]
- Anosmia [HPO term]
- Congenital ichthyosiform erythroderma [HPO term]
- Congenital ichthyosis [HPO term]
- Gonadotropin deficiency [HPO term]
- Gonadotropin deficiency [HPO term]
- Hyperchromic macrocytic anemia [HPO term]
- Hypogonadotropic hypogonadism [HPO term]
- Intellectual disability [HPO term]
- Male hypogonadism [HPO term]
- Polyneuritis [HPO term]
- Rod-cone dystrophy [HPO term]
- Seizure [HPO term]
- X-linked inheritance [HPO term]
ORDO concept(s)
- Ichthyosis-male hypogonadism syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ichthyosis and male hypogonadism [MeSH concept]
- Ichthyosis-male hypogonadism syndrome [ORDO Disease]
- ichthyosis and male hypogonadism [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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