|
Walker-Warburg syndrome or muscle-eye-brain disease, Fktn-Related
|
http://purl.obolibrary.org/obo/MONDO_0009678 |
|
|
autosomal recessive parkinson disease 14
|
C567844 |
|
|
complete or partial, with 9p24.3 deletion 46,xy gonadal dysgenesis
|
C567887 |
|
|
pain syndrome, patellofemoral
|
D046788 |
|
|
absent middle phalanges of digits 2-5 with nail dysplasia
|
19678 |
|
|
nonsyndromic, autosomal recessive male infertility
|
C567832 |
|
|
obsolete glycoprotein, renal
|
7678.0 |
|
|
disease with punctate palmoplantar hyperkeratosis as a major feature
|
http://purl.obolibrary.org/obo/MONDO_0017678 |
|
|
disease with punctate palmoplantar keratoderma as a major feature
|
http://purl.obolibrary.org/obo/MONDO_0017678 |
|
|
incomplete molar pregnancy
|
16786 |
|
|
familial, with prenatal or early onset convulsive disorder
|
C565678 |
|
|
charlevoix-saguenay type spastic ataxia
|
C536787 |
|
