MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы

Matthew-Wood syndrome

ORPHA:2470Порок
Autosomal dominant, Autosomal recessive

Maxillonasal dysplasia

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

May-Thurner syndrome

ORPHA:675404Заболевание
Not applicable

Mayer-Rokitansky-Küster-Hauser syndrome

ORPHA:3109Порок
Autosomal dominant, Not applicable

Mayer-Rokitansky-Küster-Hauser syndrome type 1

ORPHA:247775Клин. подт.
Autosomal dominant, Not applicable

Mayer-Rokitansky-Küster-Hauser syndrome type 2

ORPHA:2578Клин. подт.
Autosomal dominant, Not applicable

Mazabraud syndrome

ORPHA:57782Порок
Not applicable

McCune-Albright syndrome

ORPHA:562Заболевание
Not applicable

McDonough syndrome

ORPHA:2471Порок

McKusick-Kaufman syndrome

ORPHA:2473Порок
Autosomal recessive

McLeod neuroacanthocytosis syndrome

ORPHA:59306Заболевание
X-linked recessive

Meacham syndrome

ORPHA:3097Порок
Autosomal dominant

Meckel syndrome

ORPHA:564Порок
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.
Not applicable

Median facial cleft

ORPHA:141234Клин. гр.

Median nodule of the upper lip

ORPHA:2699Порок
Autosomal dominant

Mediastinal arteriovenous malformation

ORPHA:714709Морф.
Not applicable

Medich giant platelet syndrome

ORPHA:370127Заболевание

Medium chain acyl-CoA dehydrogenase deficiency

ORPHA:42Заболевание
Autosomal recessive

Medullary sponge kidney

ORPHA:1309Морф.
Autosomal dominant, Not applicable

Medullary thyroid carcinoma

ORPHA:1332Заболевание
Not applicable

Medulloblastoma

ORPHA:616Заболевание
Not applicable