Eunuchoid habitus

Symptom Information:

Symptom ID: HPO:0003782
Synonyms:
Eunuchoidism [HPO:0003782]
Eunuchoid habitus [OMIM:Eunuchoid habitus]
Eunochoid morphotype [Orphanet:53850]
Eunuchoidism [OMIM:Eunuchoidism]
Eunuchoidism [MedDRA:10015532]
Quality:
Cross references:
Orphanet:53850 "Eunochoid morphotype" [Orphanet:53850]
OMIM: "Eunuchoid habitus" [OMIM:Eunuchoid habitus]
OMIM: "Eunuchoidism" [OMIM:Eunuchoidism]
UMLS:C0151721 "Eunuchoidism" [HPO:0003782]
Is a (Direct Parents):
Orphanet Build/stature/longevity anomalies
HPO         Abnormality of body weight
MedDRA Testicular and epididymal disorders NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Growth abnormality(HPO:0001507)
          Abnormality of body weight(HPO:0004323)
             Eunuchoid habitus(HPO:0003782)
MedDRA:
Reproductive system and breast disorders(MedDRA:10038604)
    Testicular and epididymal disorders(MedDRA:10013362)
       Testicular and epididymal disorders NEC(MedDRA:10043296)
          Eunuchoid habitus(HPO:0003782)
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

46,XY complete gonadal dysgenesis (Orphanet:242)
Aromatase deficiency (Orphanet:91)
HYPOGONADISM WITH LOW-GRADE MENTAL DEFICIENCY AND MICROCEPHALY (OMIM:241000)
HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA (OMIM:308700)
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus (Orphanet:3044)
KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA (OMIM:308750)
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies (Orphanet:2234)
Urban-Rogers-Meyer syndrome (Orphanet:3409)