Lipoatrophy

Symptom Information:

Symptom ID: HPO:0100578
Synonyms:
Lipoatrophy (disorder) [Orphanet:23440]
Lipoatrophy [Orphanet:23440]
Lipoatrophy [MedDRA:10024604]
Fat atrophy [MedDRA:10024604]
Fat atrophy NOS [MedDRA:10024604]
Limb lipoatrophy [MedDRA:10024604]
Lipoatrophy (lower face, upper limb, buttock) [OMIM:Lipoatrophy (lower face, upper limb, buttock)]
Quality:
Cross references:
Orphanet:23440 "Lipoatrophy" [Orphanet:23440]
OMIM: "Lipoatrophy (lower face, upper limb, buttock)" [OMIM:Lipoatrophy (lower face, upper limb, buttock)]
UMLS:C1280433 "Lipoatrophy" [HPO:0100578]
UMLS:C1280433 "Lipoatrophy" [Orphanet:23440]
Is a (Direct Parents):
HPO         Lipodystrophy
Orphanet Abnormality of the skin
MedDRA Generalized lipodystrophy
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)
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)