Lipoatrophy
Symptom Information:
Symptom ID: | HPO:0100578 | |||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of connective tissue(HPO:0003549) Abnormality of adipose tissue(HPO:0009124) Lipodystrophy(HPO:0009125) Lipoatrophy(HPO:0100578) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin and subcutaneous tissue disorders NEC(MedDRA:10040790) Generalized lipodystrophy(HPO:0009064) Lipoatrophy(HPO:0100578) |
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Database Frequency: | 30 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
AREDYLD syndrome | (Orphanet:1133) |
Acro-osteolysis-keloid-like lesions-premature aging syndrome | (Orphanet:363665) |
Acrogeria | (Orphanet:2500) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Bird headed-dwarfism, Montreal type | (Orphanet:2617) |
Congenital short bowel syndrome | (Orphanet:2301) |
DK1-CDG | (Orphanet:91131) |
Ectodermal dysplasia, tricho-odonto-onychial type | (Orphanet:1818) |
Familial isolated dilated cardiomyopathy | (Orphanet:154) |
Familial partial lipodystrophy associated with PLIN1 mutations | (Orphanet:280356) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Familial partial lipodystrophy, Köbberling type | (Orphanet:79084) |
Fucosidosis | (Orphanet:349) |
Leprechaunism | (Orphanet:508) |
Lipodystrophy - intellectual deficit - deafness | (Orphanet:50811) |
Lipodystrophy due to peptidic growth factors deficiency | (Orphanet:1979) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Marfanoid habitus - intellectual deficit, autosomal recessive | (Orphanet:2463) |
Multifocal muscular fibrosis - obstructed vessels | (Orphanet:2033) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Nestor-Guillermo progeria syndrome | (Orphanet:280576) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Progeroid syndrome, Petty type | (Orphanet:2963) |
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications | (Orphanet:3018) |
SHORT syndrome | (Orphanet:3163) |
Say-Barber-Miller syndrome | (Orphanet:3132) |
Stiff skin syndrome | (Orphanet:2833) |
Weaver-Williams syndrome | (Orphanet:3448) |
Werner syndrome | (Orphanet:902) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |