MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Macrodactyly of toes, unilateral

ORPHA:295243Клин. под.
Autosomal dominant

Macrophage activation syndrome

ORPHA:158061Clinical syndrome

Macrophagic myofasciitis

ORPHA:592Ауру
Not applicable

Macrosomia-microphthalmia-cleft palate syndrome

ORPHA:2432Мальф.

Macrostomia-preauricular tags-external ophthalmoplegia syndrome

ORPHA:83619Мальф.
Autosomal dominant

Macrothrombocytopenia with mitral valve insufficiency

ORPHA:220448Ауру

Macular coloboma-cleft palate-hallux valgus syndrome

ORPHA:91494Мальф.
Autosomal recessive

Macular corneal dystrophy

ORPHA:98969Ауру
Autosomal recessive

Maculopapular cutaneous mastocytosis

ORPHA:79457Ауру
Not applicable

Madras motor neuron disease

ORPHA:137867Ауру
Not applicable, X-linked recessive

Maffucci syndrome

ORPHA:163634Ауру
Not applicable

Majeed syndrome

ORPHA:77297Ауру
Autosomal recessive

Mal de Meleda

ORPHA:87503Ауру
Autosomal recessive

Mal de débarquement

ORPHA:210272Clinical syndrome
Not applicable

Malakoplakia

ORPHA:556Ауру
Unknown

Malan overgrowth syndrome

ORPHA:420179Мальф.
Autosomal dominant, Unknown

Malaria

ORPHA:673Ауру
Not applicable

Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome

ORPHA:2234Мальф.
Unknown

Male infertility due to acephalic spermatozoa

ORPHA:529970Клин. под.
Autosomal recessive

Male infertility due to globozoospermia

ORPHA:171709Клин. под.
Autosomal recessive

Male infertility due to large-headed multiflagellar polyploid spermatozoa

ORPHA:137893Клин. под.
Autosomal recessive

Male infertility with azoospermia or oligozoospermia due to single gene mutation

ORPHA:399805Ауру
Autosomal dominant, Autosomal recessive, X-linked recessive

Male infertility with teratozoospermia due to single gene mutation

ORPHA:399808Ауру

Malformation of the neurenteric canal, spinal cord and column

ORPHA:268843Сан.