Reduced subcutaneous adipose tissue

Symptom Information:

Symptom ID: HPO:0003758
Synonyms:
Decreased subcutaneous adipose tissue [HPO:0003758]
Reduced subcutaneous fat [HPO:0003758]
Scanty adipose tissue [HPO:0003758]
Decreased subcutaneous adipose tissue [OMIM:Decreased subcutaneous adipose tissue]
Reduced subcutaneous fat [OMIM:Reduced subcutaneous fat]
Scanty adipose tissue [OMIM:Scanty adipose tissue]
Quality:
Cross references:
OMIM: "Decreased subcutaneous adipose tissue" [OMIM:Decreased subcutaneous adipose tissue]
OMIM: "Reduced subcutaneous fat" [OMIM:Reduced subcutaneous fat]
OMIM: "Scanty adipose tissue" [OMIM:Scanty adipose tissue]
Is a (Direct Parents):
HPO         Abnormality of adipose tissue
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of connective tissue(HPO:0003549)
          Abnormality of adipose tissue(HPO:0009124)
             Reduced subcutaneous adipose tissue(HPO:0003758)
MedDRA:
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

19q13.11 microdeletion syndrome (Orphanet:217346)
ANE syndrome (Orphanet:157954)
AREDYLD syndrome (Orphanet:1133)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME B (OMIM:133540)
Camurati-Engelmann disease (Orphanet:1328)
Cockayne syndrome (Orphanet:191)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Focal facial dermal dysplasia (Orphanet:79133)
Fumaric aciduria (Orphanet:24)
GRANDDAD SYNDROME (OMIM:138920)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Glomerulonephritis - sparse hair - telangiectasis (Orphanet:2087)
Glomerulonephritis - sparse hair - telangiectasis (Orphanet:2087)
Glycogen storage disease due to GLUT2 deficiency (Orphanet:2088)
Insulin-resistance syndrome type A (Orphanet:2297)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3 (OMIM:612526)
LMNA-related cardiocutaneous progeria syndrome (Orphanet:363618)
Lipodystrophy due to peptidic growth factors deficiency (Orphanet:1979)
MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGEDAPPEARANCE (OMIM:248010)
Mandibuloacral dysplasia (Orphanet:2457)
Marfan syndrome type 1 (Orphanet:284963)
Marfanoid habitus - intellectual deficit, autosomal recessive (Orphanet:2463)
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES (OMIM:602249)
ROWLEY-ROSENBERG SYNDROME (OMIM:268500)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)