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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Hypochondrogenesis

ORPHA:93297Клин. под.
Autosomal dominant

Hypochondroplasia

ORPHA:429Ауру
Autosomal dominant

Hypocomplementemic urticarial vasculitis

ORPHA:36412Ауру
Autosomal recessive, Not applicable

Hypodontia-dysplasia of nails syndrome

ORPHA:2228Мальф.
Autosomal dominant

Hypodontia-scalp hypotrichosis-facial dysmorphism syndrome

ORPHA:685067Ауру
Autosomal recessive

Hypoglossia-hypodactyly syndrome

ORPHA:989Мальф.
Unknown

Hypogonadism-mitral valve prolapse-intellectual disability syndrome

ORPHA:2233Ауру
Unknown

Hypogonadotropic hypogonadism-frontoparietal alopecia syndrome

ORPHA:2230Ауру
Autosomal dominant

Hypogonadotropic hypogonadism-retinitis pigmentosa syndrome

ORPHA:2235Ауру
Unknown

Hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome

ORPHA:293967Мальф.
Autosomal recessive

Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome

ORPHA:528105Ауру
Autosomal recessive

Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome

ORPHA:363523Ауру
Autosomal recessive

Hypohidrotic ectodermal dysplasia

ORPHA:238468Ауру
Autosomal dominant, Autosomal recessive, X-linked recessive

Hypohidrotic ectodermal dysplasia with immunodeficiency

ORPHA:98813Ауру
Autosomal dominant, X-linked recessive

Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome

ORPHA:1882Мальф.
Autosomal recessive

Hypohidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome

ORPHA:69088Ауру
X-linked recessive

Hypoinsulinemic hypoglycemia and body hemihypertrophy

ORPHA:293964Ауру
Autosomal dominant

Hypokalemic periodic paralysis

ORPHA:681Ауру
Autosomal dominant

Hypomandibular faciocranial dysostosis

ORPHA:1790Мальф.
Unknown

Hypomaturation amelogenesis imperfecta

ORPHA:100033Клин. под.
Autosomal recessive, X-linked dominant

Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism

ORPHA:100034Клин. под.
Autosomal dominant

Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome

ORPHA:137639Клин. под.
Autosomal recessive

Hypomyelination neuropathy-arthrogryposis syndrome

ORPHA:2680Мальф.
Autosomal recessive

Hypomyelination of early myelinating structures

ORPHA:599376Ауру
X-linked dominant