MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Matthew-Wood syndrome

ORPHA:2470Мальформация
Autosomal dominant, Autosomal recessive

Maxillonasal dysplasia

ORPHA:1248Мальформация
Autosomal dominant, Autosomal recessive, Multigenic/multifactorial

May-Thurner syndrome

ORPHA:675404Заболевание
Not applicable

Mayer-Rokitansky-Küster-Hauser syndrome

ORPHA:3109Мальформация
Autosomal dominant, Not applicable

Mayer-Rokitansky-Küster-Hauser syndrome type 1

ORPHA:247775Клин. подтип
Autosomal dominant, Not applicable

Mayer-Rokitansky-Küster-Hauser syndrome type 2

ORPHA:2578Клин. подтип
Autosomal dominant, Not applicable

Mazabraud syndrome

ORPHA:57782Мальформация
Not applicable

McCune-Albright syndrome

ORPHA:562Заболевание
Not applicable

McDonough syndrome

ORPHA:2471Мальформация

McKusick-Kaufman syndrome

ORPHA:2473Мальформация
Autosomal recessive

McLeod neuroacanthocytosis syndrome

ORPHA:59306Заболевание
X-linked recessive

Meacham syndrome

ORPHA:3097Мальформация
Autosomal dominant

Meckel syndrome

ORPHA:564Мальформация
Autosomal recessive

Meconium aspiration syndrome

ORPHA:70588Заболевание
Not applicable

Medial condensing osteitis of the clavicle

ORPHA:57196Заболевание
Not applicable

Median cleft lip/mandible

ORPHA:2006Морф. аномалия
Not applicable

Median facial cleft

ORPHA:141234Клин. группа

Median nodule of the upper lip

ORPHA:2699Мальформация
Autosomal dominant

Mediastinal arteriovenous malformation

ORPHA:714709Морф. аномалия
Not applicable

Medich giant platelet syndrome

ORPHA:370127Заболевание

Medium chain acyl-CoA dehydrogenase deficiency

ORPHA:42Заболевание
Autosomal recessive

Medullary sponge kidney

ORPHA:1309Морф. аномалия
Autosomal dominant, Not applicable

Medullary thyroid carcinoma

ORPHA:1332Заболевание
Not applicable

Medulloblastoma

ORPHA:616Заболевание
Not applicable