Clinical and research tests for Bellucia nigricans - Genetic Testing Registry (GTR)

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Select all conditions on this page	Conditions	Synonyms
Select item 394201	Crouzon syndrome-acanthosis nigricans syndrome	CROUZONODERMOSKELETAL SYNDROME Crouzon syndrome with acanthosis nigricans
Select item 501111	Insulin-resistant diabetes mellitus AND acanthosis nigricans	DIABETES MELLITUS, INSULIN-RESISTANT, WITH ACANTHOSIS NIGRICANS, TYPE A Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans INSULIN RECEPTOR, DEFECT IN, WITH INSULIN-RESISTANT DIABETES MELLITUS AND ACANTHOSIS NIGRICANS IRAN, TYPE A Insulin-resistance syndrome type A type A insulin resistance
Select item 393098	Severe achondroplasia-developmental delay-acanthosis nigricans syndrome	SADDAN dysplasia SSB syndrome Severe achondroplasia with developmental delay and acanthosis nigricans Skeleton skin brain syndrome
Select item 865175	Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension	Insulin resistance, digenic
Select item 78675	Alstrom syndrome	Alstrom's syndrome
Select item 354526	Familial partial lipodystrophy, Dunnigan type	Familial partial lipodystrophy 2 Lipodystrophy, familial, of limbs and lower trunk Lipodystrophy, reverse partial Partial lipodystrophy, Dunnigan
Select item 377668	Beare-Stevenson cutis gyrata syndrome	Beare-Stevenson Syndrome Cutis Gyrata syndrome of Beare and Stevenson
Select item 328393	PPARG-related familial partial lipodystrophy	Familial partial lipodystrophy 3 LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS
Select item 334042	Lelis syndrome	Ectodermal dysplasia, hypohidrotic, with acanthosis nigricans
Select item 1675945	PLIN1-related familial partial lipodystrophy	Familial partial lipodystrophy 4 LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PLIN1 MUTATIONS
Select item 340317	Retinitis pigmentosa-intellectual disability-deafness-hypogenitalism syndrome	Insulin-resistant diabetes with acanthosis nigricans, hypogonadism, pigmentary retinopathy, deafness, and mental retardation Retinitis pigmentosa, deafness, mental retardation, and hypogonadism
Select item 348051	Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome	Acanthosis nigricans with muscle cramps and acral enlargement Familial insulin resistance with acanthosis nigricans, acral hypertrophy and muscle cramps
Select item 815270	CIDEC-related familial partial lipodystrophy	Familial partial lipodystrophy 5 LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH CIDEC MUTATIONS
Select item 54	Acanthosis nigricans
Select item 124408	Familial partial lipodystrophy
Select item 1631964	Ring chromosome Y
Select item 472991	Papillomatosis, confluent and reticulated	PAPILLOMATOSIS, RETICULATED AND CONFLUENT, OF GOUGEROT AND CARTEAUD
Select item 371331	Ectodermal dysplasia with natal teeth, Turnpenny type	ECTODERMAL DYSPLASIA, HAIR/TOOTH TYPE
Select item 1810936	AKT2-related familial partial lipodystrophy
Select item 1806985	Microcephalic primordial dwarfism-insulin resistance syndrome

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