Acanthosis nigricans

Symptom Information:

Symptom ID: HPO:0000956
Synonyms:
Acanthosis (morphologic abnormality) [Orphanet:23560]
Acanthosis nigricans (disorder) [Orphanet:23560]
Acanthosis [Orphanet:23560]
Acanthosis Nigricans [Orphanet:23560]
Acanthosis nigricans [OMIM:Acanthosis nigricans]
Acanthosis nigricans [Orphanet:23560]
Acanthosis nigricans [MedDRA:10000350]
Acquired acanthosis nigricans [MedDRA:10000350]
Acanthosis [MedDRA:10000349]
Acanthosis [OMIM:Acanthosis]
Acanthosis nigricans (in some patients) [OMIM:Acanthosis nigricans (in some patients)]
Acanthosis nigricans (uncommon) [OMIM:Acanthosis nigricans (uncommon)]
Quality:
Cross references:
Orphanet:23560 "Acanthosis nigricans" [Orphanet:23560]
OMIM: "Acanthosis nigricans" [OMIM:Acanthosis nigricans]
OMIM: "Acanthosis" [OMIM:Acanthosis]
OMIM: "Acanthosis nigricans (in some patients)" [OMIM:Acanthosis nigricans (in some patients)]
OMIM: "Acanthosis nigricans (uncommon)" [OMIM:Acanthosis nigricans (uncommon)]
UMLS:C0221270 "Acanthosis" [Orphanet:23560]
UMLS:C0000889 "Acanthosis Nigricans" [Orphanet:23560]
Is a (Direct Parents):
HPO         Epidermal thickening
Orphanet Abnormality of skin pigmentation
MedDRA Paraneoplastic syndromes NEC
MedDRA Skin hyperplasias and hypertrophies
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of skin morphology(HPO:0011121)
                   Thickened skin(HPO:0001072)
                      Epidermal thickening(HPO:0011368)
                         Acanthosis nigricans(HPO:0000956)
MedDRA:
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Neoplasm related morbidities(MedDRA:10068775)
       Paraneoplastic syndromes NEC(MedDRA:10067229)
          Acanthosis nigricans(HPO:0000956)
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Cornification and dystrophic skin disorders(MedDRA:10011063)
       Skin hyperplasias and hypertrophies(MedDRA:10040866)
          Acanthosis nigricans(HPO:0000956)
Database Frequency: 54 / 7739
Resource:

All diseases associated with this symptom:

Absence of fingerprints - congenital milia (Orphanet:1658)
Acanthosis nigricans (Orphanet:924)
Acanthosis nigricans - Insulin resistance - muscle cramps - acral enlargement (Orphanet:90301)
Achondroplasia (Orphanet:15)
Acquired hypertrichosis lanuginosa (Orphanet:2221)
Acrokeratosis verruciformis of Hopf (Orphanet:79151)
Acromegaly (Orphanet:963)
Alström syndrome (Orphanet:64)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Bardet-Biedl syndrome 10 (OMIM:615987)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
CORTISONE REDUCTASE DEFICIENCY 2 (OMIM:614662)
Cabezas syndrome (Orphanet:85293)
Congenital reticular ichthyosiform erythroderma (Orphanet:281190)
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis (Orphanet:352662)
Costello syndrome (Orphanet:3071)
Crouzon disease (Orphanet:207)
Crouzon syndrome - acanthosis nigricans (Orphanet:93262)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
Diffuse palmoplantar keratoderma with painful fissures (Orphanet:369999)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ectodermal dysplasia with natal teeth, Turnpenny type (Orphanet:69083)
Exfoliative ichthyosis (Orphanet:289586)
Familial partial lipodystrophy associated with PLIN1 mutations (Orphanet:280356)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
Familial partial lipodystrophy due to AKT2 mutations (Orphanet:79085)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Familial partial lipodystrophy, Köbberling type (Orphanet:79084)
Focal palmoplantar keratoderma with joint keratoses (Orphanet:370002)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Generalized pustular psoriasis (Orphanet:247353)
Hypopigmentation-punctate palmoplantar keratoderma syndrome (Orphanet:324561)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2 (OMIM:242100)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8 (OMIM:613943)
Ichthyosis - hypotrichosis - sclerosing cholangitis (Orphanet:59303)
Insulin-resistance syndrome type A (Orphanet:2297)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 (OMIM:608594)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3 (OMIM:612526)
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5 (OMIM:615238)
Leprechaunism (Orphanet:508)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mulibrey nanism (Orphanet:2576)
Naxos disease (Orphanet:34217)
Netherton syndrome (Orphanet:634)
Neuroectodermal-endocrine syndrome (Orphanet:2676)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Rabson-Mendenhall syndrome (Orphanet:769)
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism (Orphanet:3085)
Sterile multifocal osteomyelitis with periostitis and pustulosis (Orphanet:210115)
Thanatophoric dysplasia (Orphanet:2655)
Thanatophoric dysplasia type 1 (Orphanet:1860)
Thanatophoric dysplasia type 2 (Orphanet:93274)