| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) |
Parent Node:
Arthrogryposis (D001176) |
..Starting node
.. Spondylohypoplasia, arthrogryposis and popliteal pterygium (C535790)
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Child Nodes:
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Sister Nodes: |
..Arthrogryposis and ectodermal dysplasia (C537441)
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..Arthrogryposis epileptic seizures migrational brain disorder (C537442)
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..Arthrogryposis multiplex congenita neurogenic type (C536614)
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..Arthrogryposis multiplex congenita whistling face (C538401)
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..Arthrogryposis multiplex congenita, distal type 1 (C535378)
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..Arthrogryposis multiplex congenita, distal type 2 (C535379)
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..Arthrogryposis multiplex congenita, distal, X-linked (C535380)
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..Arthrogryposis multiplex with deafness, inguinal hernias, and early death (C535381)
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..Arthrogryposis renal dysfunction cholestasis syndrome (C535382)
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..ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED (OMIM:300158)
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..Arthrogryposis, Distal, Type 10 (C566069)
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..ARTHROGRYPOSIS, DISTAL, TYPE 1A (OMIM:108120)
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..Arthrogryposis, distal, type 2E (C535384)
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..Arthrogryposis, Distal, Type 4 (C563791)
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..Arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies (C535385)
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..Arthrogryposis, Distal, with Mental Retardation and Characteristic Facies (C565940)
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..Arthrogryposis, X-Linked, Type V (C564574)
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..Arthrogryposis-like hand anomaly and sensorineural deafness (C535386)
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..Boylan Dew Greco syndrome (C537083)
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..Bruck syndrome 1 (C537406)
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..Bruck syndrome 2 (C537407)
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..Camptodactyly-ichthyosis syndrome (C537976)
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..Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome (C566861)
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..Cerebrooculofacioskeletal Syndrome 2 (C565185)
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..Cerebrooculofacioskeletal Syndrome 4 (C565184)
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..Contractures ectodermal dysplasia cleft lip palate (C535465)
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..Cyprus facial neuromusculoskeletal syndrome (C536229)
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..Distal arthrogryposis Moore Weaver type (C536814)
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..Distal arthrogryposis type 2B (C538400)
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..EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 (OMIM:601776)
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..German Syndrome (C562543)
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..Gordon syndrome (C537288)
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..Hecht syndrome (C535857)
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..Holoprosencephaly with Fetal Akinesia/Hypokinesia Sequence (C564409)
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..Jequier Kozlowski skeletal dysplasia (C537569)
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..Johnston Aarons Schelley syndrome (C535883)
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..Kuskokwim disease (C538124)
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..Ladda Zonana Ramer syndrome (C538135)
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..Lethal Arthrogryposis With Anterior Horn Cell Disease (C567502)
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..Lethal congenital contracture syndrome 1 (C537194)
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..Lethal Congenital Contracture Syndrome 2 (C564369)
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..Massa Casaer Ceulemans syndrome (C536031)
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..Minicore myopathy, antenatal onset, with arthrogryposis (C537474)
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..Multiple Pterygium Syndrome, Autosomal Dominant (C566739)
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..MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE (OMIM:253290)
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..Muscular Dystrophy, Congenital, Producing Arthrogryposis (C564985)
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..Neuropathy, congenital, with arthrogryposis multiplex (C535714)
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..Oculomelic amyoplasia (C537737)
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..Pelvic dysplasia arthrogryposis of lower limbs (C535548)
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..Pena Shokeir syndrome, type 1 (C536647)
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..Podder-Tolmie syndrome (C537518)
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..Ray Peterson Scott syndrome (C535292)
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..Spondylohypoplasia, arthrogryposis and popliteal pterygium (C535790)
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..Spranger Schinzel Myers syndrome (C535801)
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..Tomaculous neuropathy (C536965)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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