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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Microcephaly-short stature-intellectual disability-facial dysmorphism syndrome

ORPHA:423306Мальф.
Autosomal recessive

Microcephaly-short stature-limb abnormalities syndrome

ORPHA:572773Клин. под.
Autosomal recessive

Microcephaly-thin corpus callosum-intellectual disability syndrome

ORPHA:397951Ауру
Autosomal recessive

Microcornea-glaucoma-absent frontal sinuses syndrome

ORPHA:2536Мальф.

Microcornea-myopic chorioretinal atrophy-telecanthus syndrome

ORPHA:369970Ауру
Autosomal recessive

Microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome

ORPHA:231736Мальф.
Unknown

Microcystic lymphatic malformation

ORPHA:79490Мальф.
Not applicable

Microcystic stromal tumor

ORPHA:569248Ауру

Microcytic anemia with liver iron overload

ORPHA:83642Ауру
Autosomal recessive

Microduplication Xp11.22p11.23 syndrome

ORPHA:217377Мальф.
Not applicable, X-linked dominant

Microform holoprosencephaly

ORPHA:280200Мальф.
Multigenic/multifactorial

Microgastria-limb reduction defect syndrome

ORPHA:2538Мальф.
Not applicable

Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome

ORPHA:476126Мальф.
Autosomal dominant

Microlissencephaly

ORPHA:1083Морф.
Autosomal recessive

Microlissencephaly-micromelia syndrome

ORPHA:50810Мальф.
Autosomal recessive

Microphthalmia with brain and digit anomalies

ORPHA:139471Мальф.
Autosomal dominant

Microphthalmia with limb anomalies

ORPHA:1106Мальф.
Autosomal recessive

Microphthalmia with linear skin defects syndrome

ORPHA:2556Мальф.
X-linked dominant

Microphthalmia, Lenz type

ORPHA:568Мальф.
X-linked recessive

Microphthalmia-ankyloblepharon-intellectual disability syndrome

ORPHA:85275Мальф.
X-linked recessive

Microphthalmia-anophthalmia-coloboma

ORPHA:98555Сан.
Autosomal dominant, Autosomal recessive, X-linked recessive

Microphthalmia-brain atrophy syndrome

ORPHA:77299Мальф.
Autosomal recessive

Microphthalmia-microtia-fetal akinesia syndrome

ORPHA:2547Мальф.

Microphthalmia-motor delay-language delay-brain anomalies-diaphragmatic hernia syndrome

ORPHA:689829Ауру
Autosomal dominant, Autosomal recessive