Acanthosis nigricans
Symptom Information:
Symptom ID: | HPO:0000956 | ||||||||||||
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 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) |
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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) |