Reduced subcutaneous adipose tissue
Symptom Information:
Symptom ID: | HPO:0003758 | ||||||
Synonyms: |
|
||||||
Quality: | |||||||
Cross references: |
|
||||||
Is a (Direct Parents): |
|
||||||
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) |